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Recalls affecting Utah

Data last updated: September 11, 2026 at 1:08 PM UTC

16,633 recalls found
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Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

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Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

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Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

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UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

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Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

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UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

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Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

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Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

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Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

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UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

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Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaE. coliAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusSalmonellaAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

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Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
Wording
UnclassifiedRisk not yet known
Medical deviceRecalled October 14, 2021

Arietta 850 Ultrasound- Software Version: V1.0.0 through V4.1.3

Diagnostic ultrasound system with the specified software version and used in conjunction with a Fujifilm (formally Hitachi) transducer does not display the measurement results correctly with two cardiology measurement functions: Mitral Regurgitation Flow (MR Flow) Measurement; Mitral Valve (MV) Measurement. In addition there is an error in the instruction manual.

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FDA has not published a risk classification for this recall yet.

Recall #:
88840
Lot/product code:
Serial Numbers: 205W3386 (01)04562122958974(11)171114(21)205W3386; 206F7900 (01)04562122958974(11)180926(21)206F7900; 206F7901 (01)04562122958974(11)180926(21)206F7901; 206F7936 (01)04562122958974(11)181113(21)206F7936; 206F7937 (01)04562122958974(11)181113(21)206F7937; 206F7940 (01)04562122958974(11)181113(21)206F7940; 206F7941 (01)04562122958974(11)181113(21)206F7941; 206F7942 (01)04562122958974(11)181113(21)206F7942; 206F7944 (01)04562122958974(11)181113(21)206F7944; 206F7945 (01)04562122958974(11)181113(21)206F7945; 206F7946 (01)04562122958974(11)181113(21)206F7946; 206F7947 (01)04562122958974(11)181114(21)206F7947; G3002552 (01)04562122958974(11)20190115(21)G3002552; G3024545 (01)04562122958974(11)190607(21)G3024545; G3037885 (01)04562122958974(11)20190719(21)G3037885; G3037887 (01)04562122958974(11)20190719(21)G3037887; G3042405 (01)04562122958974(11)190829(21)G3042405; G3042823 (01)04562122958974(11)20190807(21)G3042823; G3042828 (01)04562122958974(11)20190808(21)G3042828; G3045094 (01)04562122958974(11)20190822(21)G3045094; G3052105 (01)04562122958974(11)20191008(21)G3052105 G3052118 (01)04562122958974(11)20191025(21)G3052118 G3055549 (01)04562122958974(11)20191118(21)G3055549 G3055550 (01)04562122958974(11)20191118(21)G3055550 G3055552 (01)04562122958974(11)20191118(21)G3055552 G3055553 (01)04562122958974(11)20191118(21)G3055553 G3055554 (01)04562122958974(11)20191118(21)G3055554 G3055555 (01)04562122958974(11)20191118(21)G3055555 G3060234 (01)04562122958974(11)20191206(21)G3060234 G3060254 (01)04562122958974(11)20191206(21)G3060254 G3060275 (01)04562122958974(11)20191216(21)G3060275 G3060278 (01)04562122958974(11)20191216(21)G3060278 G3060690 (01)04562122958974(11)200127(21)G3060690 G3071074 (01)04562122958974(11)20200227(21)G3071074 G3080785 (01)04562122958974(11)201105(21)G3080785 G3090450 (01)04562122958974(11)201225(21)G3090450 G3110884 (01)04562122958974(11)210401(21)G3110884
Recalling firm:
FujiFilm Healthcare Americas Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 15, 2021

Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE

During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube

ALL 50 STATES
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FDA has not published a risk classification for this recall yet.

Recall #:
88951
Lot/product code:
Model Number/Product Descripton: ENTF2525C70EE/STENT GRAFT ENTF2525C70EE ENDURANT TUBE GTIN Code: 00763000006129 Serial Numbers: V30624638 V30624639
Recalling firm:
Medtronic Vascular, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 15, 2021

Endurant II Stent Graft System REF/Description: ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE STENT GRAFT ETBF2820C166EE ENDUR II BIF ETCF2828C49EE STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETCF2828C49EE STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETCF2828C49EE STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETUF2514C102EE STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE STENT GRAFT ETUF2514C102EE ENDUR II AUI ETBF2313C124EE STENT GRAFT ETBF2313C124EE ENDUR II BIF ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2513C145EE STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2516C166EE STENT GRAFT ETBF2516C166EE ENDUR II BIF ETBF2516C166EE STENT GRAFT ETBF2516C166EE ENDUR II BIF ETBF2516C166EE STENT GRAFT ETBF2516C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE STENT GRAFT ETBF2516C145EE ENDUR II BIF ETUF2514C102E STENT GRAFT ETUF2514C102E ENDUR II AUI ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETCF2525C49E STENT GRAFT ETCF2525C49E ENDUR II AOEXT ETCF2828C49E STENT GRAFT ETCF2828C49E ENDUR II AOEXT ETCF2828C49E STENT GRAFT ETCF2828C49E ENDUR II AOEXT ETCF2828C49E STENT GRAFT ETCF2828C49E ENDUR II AOEXT ETUF2814C102E STENT GRAFT ETUF2814C102E ENDUR II AUI ETUF2814C102E STENT GRAFT ETUF2814C102E ENDUR II AUI ETTF2525C70EE STENT GRAFT ETTF2525C70EE ENDUR II TUBE ETTF2525C70EE STENT GRAFT ETTF2525C70EE ENDUR II TUBE ETTF2525C70EE STENT GRAFT ETTF2525C70EE ENDUR II TUBE ETTF2525C70EE STENT GRAFT ETTF2525C70EE ENDUR II TUBE ETTF2525C70EE STENT GRAFT ETTF2525C70EE ENDUR II TUBE ETTF2525C70EE STENT GRAFT ETTF2525C70EE ENDUR II TUBE ETBF2313C166EE STENT GRAFT ETBF2313C166EE ENDUR II BIF ETBF2513C124EE STENT GRAFT ETBF2513C124EE ENDUR II BIF ET

Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88951
Lot/product code:
Model Number/GTIN Code/Product Description: ETBF2513C145EE 00643169781047 V30584649 STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593589 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593590 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593591 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593592 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593593 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593594 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETBF2820C166EE 00643169781177 V30593595 STENT GRAFT ETBF2820C166EE ENDUR II BIF ETCF2828C49EE 00643169780798 V30595328 STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETCF2828C49EE 00643169780798 V30595331 STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETCF2828C49EE 00643169780798 V30595332 STENT GRAFT ETCF2828C49EE ENDUR II CUFF ETUF2514C102EE 00643169780934 V30595382 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595383 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595386 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595389 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595390 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETUF2514C102EE 00643169780934 V30595391 STENT GRAFT ETUF2514C102EE ENDUR II AUI ETBF2313C124EE 00643169780972 V30595456 STENT GRAFT ETBF2313C124EE ENDUR II BIF ETBF2513C145EE 00643169781047 V30595505 STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2513C145EE 00643169781047 V30595515 STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2513C145EE 00643169781047 V30595516 STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2513C145EE 00643169781047 V30595517 STENT GRAFT ETBF2513C145EE ENDUR II BIF ETBF2516C166EE 00643169781085 V30596585 STENT GRAFT ETBF2516C166EE ENDUR II BIF ETBF2516C166EE 00643169781085 V30596586 STENT GRAFT ETBF2516C166EE ENDUR II BIF ETBF2516C166EE 00643169781085 V30596587 STENT GRAFT ETBF2516C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596625 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596626 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596634 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596635 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596637 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596639 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596640 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596641 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2813C166EE 00643169781115 V30596644 STENT GRAFT ETBF2813C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596645 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596646 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596648 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596649 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596650 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596651 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2816C166EE 00643169781146 V30596655 STENT GRAFT ETBF2816C166EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603296 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603298 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603309 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603310 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603311 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603312 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603313 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETBF2516C145EE 00643169781078 V30603315 STENT GRAFT ETBF2516C145EE ENDUR II BIF ETUF2514C102E 00643169232570 V30608080 STENT GRAFT ETUF2514C102E ENDUR II AUI ETTF2828C70EE 00643169780897 V30609554 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609556 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609557 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609558 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609559 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609560 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609561 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETTF2828C70EE 00643169780897 V30609564 STENT GRAFT ETTF2828C70EE ENDUR II TUBE ETCF2525C49E 00613994991430 V30616355 STENT GRAFT ETCF2525C49E ENDUR II AOEXT ETCF2828C49E 00613994991447 V30616364 STENT GRAFT ETCF2828C49E ENDUR II AOEXT ETCF2828C49E 00613994991447 V30616365 STENT GRAFT ETCF2828C49E ENDUR II AOEXT ETCF2828C49E 00613994991447 V30616368 STENT GRAFT ETCF2828C49E ENDUR II AOEXT ETUF2814C102E 00… (truncated, 33700 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Vascular, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 15, 2021

Endurant IIs Stent Graft System REF/Description: ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EJ STENT GRAFT ESBF2814C103EJ ENDUR IIS BIF ESBF2814C103EJ STENT GRAFT ESBF2814C103EJ ENDUR IIS BIF ESBF2814C103EJ STENT GRAFT ESBF2814C103EJ ENDUR IIS BIF ESBF2314C103E Stent Graft ESBF2314C103E Endur IIs BIF ESBF2314C103E Stent Graft ESBF2314C103E Endur IIs BIF ESBF2314C103E Stent Graft ESBF2314C103E Endur IIs BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2514C103EE STENT GRAFT ESBF2514C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE STENT GRAFT ESBF231

Due to, during stent graft deployment, the spindle may detach from the distal end of the spindle hypotube.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88951
Lot/product code:
Model Number/GTIN Code/Product Description: ESBF2814C103EE 00643169780446 V30609409 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609410 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609411 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609412 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609415 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609417 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609420 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609421 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30609423 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EJ 00643169440029 V30616743 STENT GRAFT ESBF2814C103EJ ENDUR IIS BIF ESBF2814C103EJ 00643169440029 V30616746 STENT GRAFT ESBF2814C103EJ ENDUR IIS BIF ESBF2814C103EJ 00643169440029 V30616748 STENT GRAFT ESBF2814C103EJ ENDUR IIS BIF ESBF2314C103E 00643169439993 V30618898 Stent Graft ESBF2314C103E Endur IIs BIF ESBF2314C103E 00643169439993 V30618899 Stent Graft ESBF2314C103E Endur IIs BIF ESBF2314C103E 00643169439993 V30618902 Stent Graft ESBF2314C103E Endur IIs BIF ESBF2814C103EE 00643169780446 V30618963 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618964 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618965 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618966 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618967 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618968 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618969 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618970 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618971 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618972 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618973 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618974 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618975 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618976 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618977 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618978 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618979 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618980 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618982 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618983 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618984 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618988 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30618989 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2514C103EE 00763000098858 V30619120 STENT GRAFT ESBF2514C103EE ENDUR IIS BIF ESBF2814C103EE 00763000098865 V30619159 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00763000098865 V30619161 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2314C103EE 00643169780422 V30625915 STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE 00643169780422 V30625916 STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE 00643169780422 V30625917 STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE 00643169780422 V30625918 STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2314C103EE 00643169780422 V30625921 STENT GRAFT ESBF2314C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625935 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625936 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625938 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625941 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625942 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625943 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625944 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625945 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625946 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625947 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625948 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625949 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625950 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625951 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643169780446 V30625952 STENT GRAFT ESBF2814C103EE ENDUR IIS BIF ESBF2814C103EE 00643… (truncated, 12383 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Vascular, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 15, 2021

GE Centricity Universal Viewer Zero Footprint Client

There is a potential to display incomplete patient imaging study.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88959
Lot/product code:
Versions 6.0 SP9, SP9.0.1, SP9.0.1.1, SP9.0.1.2, SP9.0.1.3, SP9.0.1.4, SP9.0.1.5, SP10, SP10.1, SP10.2, SP10.2.1, SP10.2.1.1, SP10.2.2, SP10.2.2.1 configured with a Centricity PACS back end. GTIN 00840682102988; UDI 00840682102988.
Recalling firm:
GE Healthcare, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 15, 2021

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD, INLINE CAMERA HEADS); 39301AS/RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES 4MM X 18CM); 39301BCTS/CAMERA TRAY (INLINE/C-MOUNT CAMERA HEADS); 39301BS/RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES 5MM X 35CM); 39301C1S/RIGID TELESCOPE TRAY (STERRAD, 1 RIGID SCOPE & LT CABLE); 39301CS/RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPE 10MM X 31CM); 39301DS/RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES); 39301HCTS/CAMERA TRAY (STERRAD, STANDARD CAMERA HEADS); 39301PHTS/CAMERA TRAY (STERRAD, PENDULUM/INLINE CAM HEADS); 39305C1S/BASKET-STYLE RIGID TELESCOPE TRAY (UDEL, 1 RIGID SCOPE 4MM X 30CM); 39305C2S/BASKET-STYLE RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES); 39305L1S/BASKET-STYLE RIGID TELESCOPE TRAY (STERRAD, 1 RIGID SCOPE); 39305L2S/BASKET-STYLE RIGID TELESCOPE TRAY (STERRAD, 2 RIGID SCOPES); 39311AS/RIGID TELESCOPE TRAY (STERRAD, 4 RIGID SCOPES & LT CABLE); 39311BS/RIGID TELESCOPE TRAY (STERRAD, TWO LAP SCOPES/CABLE); 39314FS/RIGID TELESCOPE TRAY (STERRAD, FOUR LAP SCOPES/CABLE); 39401AS/FLEXIBLE ENDOSCOPE TRAY (UP TO 39CM); 39402AS/FLEXIBLE ENDOSCOPE TRAY (FIBERSCOPES); 39403AS/FLEXIBLE ENDOSCOPE TRAY (CCD VIDESCOPES); 39406AS/FLEXIBLE ENDOSCOPE TRAY (CMOS VIDEOSCOPES)

To ensure sterilization effectiveness, sterilization tray instructions for use were updated and now state 1) udel trays may be used with flexible endoscopes with lumen diameters greater-than-or-equal to 1.2mm and maximum length of 845mm and 2) ethylene oxide is excluded as a sterilization modality.

AKALARAZCACOCTDCDEFLGAGUHIIAIDILINKSKYLAMAMDMEMIMNMOMPMSMTNCNDNENHNJNMNVNYOHOKORPAPRRISCSDTNTXUTVAVIVTWAWIWVWY
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88998
Lot/product code:
All lots with Instructions for Use Prior to PI-000078-10.0 (06/21)
Recalling firm:
Karl Storz Endoscopy
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 19, 2021

Model B35200 - Percept PC BrainSense Implantable Neurostimulator

During cardioversion events, the Model B35200 Percept PC Implantable Neurostimulator could become unresponsive and non-functional. Cardioversion is a procedure performed by a cardiologist to correct an abnormal heartbeat. Medtronic has determined that the cardioversion may damage the circuit electronics in the Percept PC stimulator, thereby, causing the Percept PC stimulator to become non-responsive.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88889
Lot/product code:
GTIN 00763000253363, Serial Numbers: NPI714835H, NPI714811H, NPI714812H, NPI714814H, NPI714816H, NPI714817H, NPI714819H, NPI714820H, NPI714750H, NPI714764H, NPI714771H, NPI714794H, NPI714682H, NPI714709H, NPI714710H, NPI714594H, NPI714598H, NPI714599H, NPI714602H, NPI714603H, NPI714606H, NPI714564H, NPI714572H, NPI714574H, NPI714587H, NPI714588H, NPI714589H, NPI714373H, NPI714379H, NPI714331H, NPI714346H, NPI714358H, NPI714378H, NPI714128H, NPI714160H, NPI714060H, NPI713947H, NPI713956H, NPI713957H, NPI714001H, NPI714017H, NPI713948H, NPI713949H, NPI713951H, NPI713952H, NPI713953H, NPI713954H, NPI713955H, NPI713829H, NPI713371H, NPI713372H, NPI713422H, NPI713242H, NPI713188H, NPI712940H, NPI712785H, NPI712637H, NPI712405H, NPI712411H, NPI712412H, NPI712341H, NPI712302H, NPI712256H, NPI711876H, NPI711841H, NPI711475H, NPI711476H, NPI710876H, NPI710765H, NPI710561H, NPI710071H, NPI709964H, NPI709680H, NPI709654H, NPI709655H, NPI709575H, NPI708692H, NPI708699H, NPI708702H, NPI708709H, NPI708675H, NPI708653H, NPI708635H, NPI708457H, NPI708415H, NPI708417H, NPI708425H, NPI708367H, NPI708376H, NPI708358H, NPI708316H, NPI708288H, NPI708289H, NPI708292H, NPI708295H, NPI708299H, NPI708300H, NPI708305H, NPI708306H, NPI708309H, NPI708258H, NPI708262H, NPI708273H, NPI708127H, NPI708128H, NPI708153H, NPI708101H, NPI708102H, NPI708103H, NPI708106H, NPI708107H, NPI708110H, NPI708112H, NPI708113H, NPI708114H, NPI708117H, NPI708118H, NPI708120H, NPI708121H, NPI708123H, NPI708124H, NPI708125H, NPI708079H, NPI708080H, NPI708082H, NPI708083H, NPI708084H, NPI708085H, NPI708086H, NPI708087H, NPI708088H, NPI708089H, NPI708090H, NPI708091H, NPI708092H, NPI708093H, NPI708094H, NPI708095H, NPI708096H, NPI708097H, NPI708100H, NPI708105H, NPI708108H, NPI708109H, NPI708116H, NPI708126H, NPI708056H, NPI708059H, NPI708060H, NPI708062H, NPI708063H, NPI708064H, NPI708065H, NPI708066H, NPI708067H, NPI708068H, NPI708070H, NPI708071H, NPI708073H, NPI708074H, NPI708076H, NPI708077H, NPI708078H, NPI708081H, NPI708014H, NPI708037H, NPI708038H, NPI708039H, NPI708040H, NPI708041H, NPI708042H, NPI708043H, NPI708044H, NPI708045H, NPI708046H, NPI708048H, NPI708049H, NPI708050H, NPI708055H, NPI708057H, NPI707998H, NPI707999H, NPI708001H, NPI708002H, NPI708003H, NPI708004H, NPI708005H, NPI708007H, NPI708008H, NPI708009H, NPI708011H, NPI708012H, NPI708013H, NPI708015H, NPI708016H, NPI708017H, NPI708018H, NPI708020H, NPI708021H, NPI708022H, NPI708023H, NPI708024H, NPI708025H, NPI708026H, NPI708027H, NPI708028H, NPI708030H, NPI708031H, NPI708033H, NPI708034H, NPI708036H, NPI707947H, NPI707955H, NPI707956H, NPI707961H, NPI707964H, NPI707970H, NPI707972H, NPI707975H, NPI707978H, NPI707979H, NPI707982H, NPI707983H, NPI707985H, NPI707986H, NPI707987H, NPI707989H, NPI707990H, NPI707991H, NPI707992H, NPI707993H, NPI707995H, NPI707996H, NPI707997H, NPI708000H, NPI707942H, NPI707943H, NPI707944H, NPI707945H, NPI707946H, NPI707948H, NPI707949H, NPI707950H, NPI707951H, NPI707952H, NPI707953H, NPI707954H, NPI707957H, NPI707958H, NPI707959H, NPI707962H, NPI707963H, NPI707966H, NPI707968H, NPI707969H, NPI707971H, NPI707974H, NPI707976H, NPI707977H, NPI707918H, NPI707919H, NPI707920H, NPI707922H, NPI707923H, NPI707924H, NPI707925H, NPI707927H, NPI707928H, NPI707929H, NPI707930H, NPI707931H, NPI707932H, NPI707934H, NPI707935H, NPI707937H, NPI707938H, NPI707939H, NPI707880H, NPI707881H, NPI707883H, NPI707884H, NPI707885H, NPI707886H, NPI707888H, NPI707890H, NPI707905H, NPI707907H, NPI707914H, NPI707916H, NPI707870H, NPI707871H, NPI707872H, NPI707873H, NPI707874H, NPI707875H, NPI707877H, NPI707879H, NPI707889H, NPI707893H, NPI707894H, NPI707895H, NPI707896H, NPI707897H, NPI707898H, NPI707899H, NPI707900H, NPI707901H, NPI707902H, NPI707846H, NPI707847H, NPI707848H, NPI707849H, NPI707856H, NPI707857H, NPI707858H, NPI707860H, NPI707861H, NPI707862H, NPI707864H, NPI707865H, NPI707867H, NPI707868H, NPI707869H, NPI707828H, NPI707830H, NPI707831H, NPI707832H, NPI707833H, NPI707834H, NPI707835H, NPI707836H, NPI707837H, NPI707838H, NPI707839H, NPI707840H, NPI707841H, NPI707842H, NPI707843H, NPI707844H, NPI707845H, NPI707851H, NPI707852H, NPI707855H, NPI707811H, NPI707812H, NPI707813H, NPI707814H, NPI707816H, NPI707818H, NPI707819H, NPI707820H, NPI707821H, NPI707822H, NPI707824H, NPI707791H, NPI707792H, NPI707794H, NPI707795H, NPI707797H, NPI707798H, NPI707799H, NPI707800H, NPI707802H, NPI707804H, NPI707805H, NPI707806H, NPI707807H, NPI707808H, NPI707809H, NPI707774H, NPI707776H, NPI707777H, NPI707779H, NPI707780H, NPI707782H, NPI707783H, NPI707784H, NPI707786H, NPI707788H, NPI707789H, NPI707790H, NPI707749H, NPI707750H, NPI707752H, NPI707753H, NPI707754H, NPI707755H, NPI707756H, NPI707757H, NPI707758H, NPI707762H, NPI707763H, NPI707764H, NPI707765H, NPI707766H, NPI707767H, NPI707768H, NPI707769H, NPI707770H, NPI707771H, NPI707772H, NPI707720H, NPI707721H, NPI707722H, NPI707723H, NPI707724H, NPI707725H, NPI707727H, NPI707728H, NPI707730H, NPI707731H, NPI707732H, NPI707733H, NPI707… (truncated, 120757 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 19, 2021

Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit IT1075-DUKE-HSP, IT1076-DUKE-HSP and IT1077-DUKE-HSP

An unreleased Version 4 Protocol Library was installed on Nimbus PainPro (H) infusion pumps in error that may impact patient safety if used on patients.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
89711
Lot/product code:
(UDI): (01)00817170020086; Lot: 2009231440; Serial Numbers: 807483, 807484, 807485, 807486, 807487, 807489, 807490, 807491, 807492, 807493, 807494, 807495, 807496, 807497, 807498, 807499, 807500, 807502, 807651, 807652, 807653, 807507, 807508, 807509, 807510, 807511, 807512, 807513, 807514, 807515, 807516, 807517, 807518, 807519, 807520, 807521, 807522, 807523, 807524, 807525, 807526, 807527, 807528, 807529, 807530, 807531, 807532, 807533, 807534, 807535, 807536, 807537, 807538, 807539, 807540, 807541, 807542, 807543, 807544, 807545, 807546, 807547, 807548, 807549, 807550, 807551, 807552, 807553, 807554, 807654, 807655, 807656, 807657, 807658
Recalling firm:
InfuTronix LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031

If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
91853
Lot/product code:
GTIN: (01)00884838076747 (Model 709030), (01)00884838101456 (Model 709031; Serial Numbers: 10000000 10000001 10000002 10000003 10000004 10000006 10000007 10000010 10000011 10000012 10000013 10000014 10000015 10000016 10000019 10000020 10000021 10000022 10000023 10000024 10000025 10000026 10000027 10000029 10000030 10000031 10000032 10000034 10000035 10000036 10000037 10000038 10000040 10000041 10000042 10000043 10000044 10000045 10000046 10000047 10000048 10000049 10000050 10000051 10000052 10000053 10000054 10000055 10000056 10000057 10000058 10000060 10000061 10000063 10000064 10000065 10000066 10000067 10000068 10000069 10000070 10000071 10000072 10000073 10000075 10000076 10000078 10000079 10000080 10000081 10000082 10000083 10000087 10000089 10000090 10000092 10000093 10000094 10000095 10000096 10000097 10000099 10000100 10000102 10000103 10000104 10000107 10000108 10000109 10000111 10000112 10000114 10000115 10000116 10000117 10000118 10000119 10000121 10000122 10000124 10000125 10000126 10000127 10000130 10000131 10000133 10000134 10000135 10000136 10000137 10000138 10000139 10000140 10000144 10000145 10000149 10000151 10000152 10000156 10000165 10000166 10000168 10000169 10000170 10000171 10000174 10000176 10000178 10000179 10000180 10000184 10000185 10000186 10000187 10000188 10000189 10000190 10000191 10000194 10000198 10000199 10000202 10001000 10001001 10001010 10001070 10001071 10001072 10001073 10001074 10001075 10001076 10001078 10001079 10001080 10001081 10001082 10001083 10001084 10001085 10001086 10001087 10001088 10001089 10001090 10001091 10001092 10001093 10001094 10001095 10001096 10001097 10001098 10001099 10001100 10001216 10001218 17000018 17000164 18000069 11201-10 24233-03 24592-122 28 7175_04 7896_04 SN16000001 SN16000002 SN16000003 SN16000004 SN16000006 SN16000007 SN16000008 SN16000009 SN17000001 SN17000002 SN17000003 SN17000004 SN17000006 SN17000007 SN17000008 SN17000009 SN17000010 SN17000011 SN17000012 SN17000013 SN17000014 SN17000015 SN17000016 SN17000017 SN17000018 SN17000019 SN17000020 SN17000021 SN17000022 SN17000023 SN17000024 SN17000101 SN17000102 SN17000103 SN17000104 SN17000105 SN17000106 SN17000107 SN17000108 SN17000109 SN17000110 SN17000111 SN17000112 SN17000113 SN17000114 SN17000115 SN17000116 SN17000117 SN17000118 SN17000119 SN17000120 SN17000121 SN17000122 SN17000123 SN17000124 SN17000126 SN17000127 SN17000128 SN17000129 SN17000130 SN17000131 SN17000132 SN17000133 SN17000134 SN17000135 SN17000136 SN17000137 SN17000138 SN17000139 SN17000140 SN17000141 SN17000142 SN17000143 SN17000144 SN17000145 SN17000146 SN17000147 SN17000148 SN17000149 SN17000150 SN17000151 SN17000152 SN17000153 SN17000154 SN17000155 SN17000156 SN17000157 SN17000158 SN17000159 SN17000160 SN17000161 SN17000162 SN17000163 SN17000164 SN17000165 SN17000166 SN17000167 SN17000168 SN17000169 SN17000170 SN17000171 SN17000227 SN18000001 SN18000002 SN18000003 SN18000004 SN18000005 SN18000006 SN18000007 SN18000008 SN18000009 SN18000010 SN18000011 SN18000012 SN18000013 SN18000014 SN18000015 SN18000016 SN18000017 SN18000018 SN18000019 SN18000020 SN18000021 SN18000022 SN18000023 SN18000024 SN18000025 SN18000026 SN18000027 SN18000028 SN18000029 SN18000030 SN18000031 SN18000032 SN18000033 SN18000034 SN18000035 SN18000036 SN18000037 SN18000038 SN18000039 SN18000041 SN18000044 SN18000045 SN18000046 SN18000047 SN18000048 SN18000049 SN18000050 SN18000051 SN18000052 SN18000053 SN18000054 SN18000055 SN18000056 SN18000057 SN18000058 SN18000060 SN18000061 SN18000062 SN18000063 SN18000064 SN18000065 SN18000066 SN18000067 SN18000068 SN18000069 SN18000070 SN18000071 SN18000072 SN18000073 SN18000074 SN18000075 SN18000076 SN18000077 SN18000078 SN18000079 SN19000001 SN19000002 SN19000003 SN19000004 SN19000005 SN19000006 SN19000007 SN19000008 SN19000009 SN19000010 SN19000011 SN19000012 SN19000013 SN19000014 SN19000015 SN19000016 SN19000017 SN19000018 SN19000019 SN19000020 SN19000021 SN19000022 SN19000023 SN19000024 SN19000025 SN19000026 SN19000027 SN19000028 SN19000029 SN19000030 SN19000031 SN19000032 SN19000033 SN19000034 SN19000035 SN19000036 SN19000037 SN19000038 SN19000039 SN19000040 SN19000041 SN19000042 10001004 10001005 10001006 10001008 10001009 10001010 10001011 10001012 10001013 10001018 10001020 10001022 10001024 10001026 10001027 10001028 10001029 10001030 10001031 10001032 10001035 10001036 10001043 10001044 10001045 10001046 10001047 10001048 10001049 10001050 10001051 10001052 10001053 10001054 10001055 10001056 10001057 10001058 10001059 10001060 10001061 10001062 10001063 10001064 10001065 10001066 10001067 10001068 10001069 10001070 10001071 10001072 10001073 10001074 10001075 10001076 10001077 10001078 10001079 10001080 10001081 10001083 10001084 10001085 10001086 10001087 10001088 10001089 10001090 10001091 10001092 10001093 10001093 10001094 10001095 10001096 10001097 10001098 10001099 10001100 10001101 10001102 10001103 10001104 10001105 10001106 10001107 10001108 10001109 10001110 10001111 10001112 1000… (truncated, 5112 characters total — see the official FDA record for the full value)
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110

If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
91853
Lot/product code:
GTIN: (01)00884838085619 (Model 706100), (01)00884838103221 (Model 709031); Serial Numbers: 597241 10000000 10000001 10000004 10000005 10000006 10000008 10000009 10000010 10000011 10000012 10000013 10000014 10000015 10000016 10000017 10000018 10000019 10000020 10000021 10000022 10000023 10000024 10000025 10000026 10000027 10000028 10000030 10000031 10000032 10000033 10000034 10000035 10000036 10000037 10000039 10000040 10000041 10000042 10000043 10000044 10000045 10000046 10000047 10000048 10000049 10000050 10000051 10000052 10000053 10000054 10000055 10001013 10001014 10001015 10001017 10001018 10001019 10001020 10001021 10001022 10001023 10001024 10001025 10001026 10001027 10001028 10001029 10001030 10001031 10001032 10001033 10001034 10001035 10001036 10001037 10001038 10001039 10001040 10001041 10001042 10001043 10001044 10001046 10001047 10001048 10001049 10001050 10001051 10001053 10001054 10001059 18000001 20000022 20000026 20000034 20000044 20000045 20000046 20000051 20000052 20000054 20000055 20000061 20000062 20000063 20000064 20000065 20000066 20000067 20000068 20000069 20000070 20000071 20000072 20000073 20000074 20000077 20000078 20000079 20000081 20000082 20000083 20000085 20000086 20000089 721815121706 SN10001000 SN10001001 SN10001002 SN10001003 SN10001004 SN10001005 SN10001006 SN10001007 SN10001008 SN10001009 SN10001010 SN10001011 SN10001012 SN18000001 SN18000002 SN18000003 SN18000004 SN18000005 SN18000006 SN18000007 SN18000008 SN18000009 SN18000011 SN18000012 SN18000013 SN18000014 SN18000015 SN18000016 SN18000017 SN18000018 SN18000019 SN18000020 SN18000021 SN18000022 SN18000023 SN18000024 SN18000152 SN18000249 SN19000001 SN19000002 SN19000003 SN19000004 SN19000005 SN19000006 SN19000007 SN19000008 SN19000009 SN19000010 SN19000011 SN19000012 SN19000013 SN19000014 SN19000015 SN19000016 SN19000017 SN19000018 10001057 10001064 10001059 10001058 10001062 10001069 10001052 10001060 10001070 10001061 10001063 10001068 10001067 10001066 10001073 10001065 10001103 10001075 10001079 10001085 10001084 10001074 10001106 10001087 10001088 10001076 10001086 10001093 10001091 10001089 10001100 10001099 10001104 10001078 10001098 10001102 10001105 10001072 10001096 10001090 10001077 10001118 10001109 10001110 10001107 10001112 10001092 10001111 10001113 10001101 10001116 10001108 10001045 10001055 10001083 10001095 10001094 10001071 10001082 10001080
Recalling firm:
Philips North America Llc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 10MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545960

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
Batches: 25608761, 25640116, 25640117, 25644834, 25649819, 25649824, 25649829, 25649834, 25678825, 25678830, 25678835, 25678839, 25678880, 25680560, 25704230, 25704231, 25704232, 25739169, 25739170, 25806714, 25819946, 25819947, 25819948, 25836147, 25836148, 25850475, 25850476, 25850477, 25850478, 25850479, 25850540, 25850541, 25878986, 25878987, 25878988, 25878989, 25878990, 25878991, 25930854, 25940128, 25940129, 25940130, 25963979, 25969161, 25969162, 25975788, 25975789, 25975790, 25975791, 26010399, 26010400, 26047895, 26047896, 26047897, 26047898, 26047899, 26048760, 26058432, 26059172, 26123198, 26123199, 26123240, 26123241, 26123242, 26123243, 26123252, 26123253, 26175502, 26175503, 26175504, 26175505, 26207999, 26208000, 26208001, 26208002, 26208003, 26240379, 26247286, 26247287, 26247288, 26247289, 26284152, 26284153, 26284154, 26284155, 26284156, 26324769, 26324771, 26324773, 26324775, 26350409, 26356442, 26366767, 26366768, 26366769, 26366770, 26366771, 26366772, 26366773, 26366774, 26406539, 26406560, 26406561, 26406562, 26435589, 26435590, 26435591, 26440046, 26457040, 26457041, 26473800, 26473801, 26489988, 26491481, 26491482, 26491483, 26491484, 26499145, 26543699, 26545849, 26545850, 26545851, 26546369, 26549973, 26559545, 26581409, 26581410, 26581827, 26600543, 26600544, 26621751, 26628098, 26638074, 26651704, 26651705, 26651706, 26651709, 26674679, 26675080, 26675081, 26677000, 26677001, 26677002, 26686240, 26696688, 26696689, 26706795, 26706796, 26706797, 26718376, 26718377, 26739329, 26739331, 26739335, 26758738, 26759340, 26759342, 26760526, 26760527, 26760528, 26760529, 26779086, 26779087, 26779088, 26779089, 26779090, 26779092, 26779093, 26808304, 26808305, 26808306, 26808307, 26848733, 26848734, 26848735, 26848736, 26848737, 26888169, 26888170, 26888171, 26888172, 26919342, 26919343, 26919344, 26919345, 26940195, 26940196, 26940197, 26940198, 26990983, 26990984, 26990985, 26990986, 26990987, 26990988, 26990989, 26990990, 26990991, 27008809, 27008810, 27008811, 27008812, 27055019, 27055120, 27062059, 27065900, 27065901, 27074115, 27074116, 27121590, 27121591, 27121596, 27121598, 27121599, 27121626, 27148639, 27148780, 27148781, 27183303, 27183304, 27183305, 27183311, 27183312, 27219848, 27220333, 27233915, 27263158, 27263159, 27265233, 27265234, 27269980, 27269981, 27269982, 27308428, 27335462, 27347597, 27347598, 27384710, 27428069 GTIN: 08714729283874 Exp. 05/18/2022 to 06/03/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 10MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545950

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
Batches: 25571372, 25673064, 25836146, 26010398, 26058426, 26123197, 26175501, 26216321, 26473779, 26759413, 26784680, 26848732, 26946145, 27121592, 27340635, 27393787 GTIN: 08714729283867 Exp. 05/09/2022 to 05/27/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 6MM 4CM- -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545920

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
GTIN: 08714729283836 Batches: 25576770, 25576881, 25576882, 25576883, 25576884, 25576885, 25608762, 25623386, 25623387, 25623388, 25623389, 25623390, 25623391, 25623392, 25623393, 25623394, 25623395, 25623396, 25623397, 25623398, 25649814, 25649817, 25649820, 25649821, 25649825, 25649826, 25649830, 25649831, 25678823, 25678827, 25678832, 25678837, 25680097, 25704217, 25704218, 25704219, 25704220, 25704221, 25704222, 25704223, 25739152, 25739153, 25739154, 25739155, 25739157, 25739158, 25771773, 25771774, 25771775, 25771776, 25771777, 25771778, 25836083, 25836084, 25836085, 25836086, 25836087, 25836088, 25836089, 25836090, 25836091, 25836092, 25878557, 25878558, 25878559, 25878980, 25878981, 25878982, 25878983, 25878984, 25878985, 25940124, 25940125, 25942723, 25947907, 25947909, 25947911, 25947913, 25947915, 25975775, 25975776, 25975777, 25975778, 25995786, 25996198, 26000471, 26000476, 26000477, 26000478, 26000479, 26000580, 26000700, 26010393, 26010394, 26010395, 26010396, 26058288, 26058291, 26058293, 26058294, 26058295, 26058296, 26058297, 26087734, 26087735, 26087736, 26087737, 26087738, 26087739, 26087740, 26087741, 26123187, 26123188, 26123189, 26123190, 26123191, 26123247, 26123248, 26123249, 26175470, 26175471, 26175472, 26175473, 26207983, 26207984, 26207985, 26207986, 26207987, 26207988, 26207989, 26207990, 26207991, 26238132, 26238133, 26238134, 26240368, 26240370, 26240371, 26240373, 26247248, 26247249, 26247250, 26247251, 26247252, 26247253, 26247254, 26247255, 26247256, 26247257, 26283632, 26283633, 26283634, 26283635, 26283636, 26283637, 26283638, 26283639, 26284140, 26284141, 26284142, 26284143, 26324749, 26324751, 26324752, 26324754, 26350404, 26350405, 26350406, 26350407, 26356444, 26366753, 26366754, 26366755, 26366756, 26366757, 26406522, 26406523, 26406524, 26406525, 26406526, 26406527, 26406528, 26406529, 26406530, 26406531, 26426921, 26426922, 26426923, 26428970, 26429811, 26429812, 26435537, 26435538, 26435539, 26435580, 26452047, 26456916, 26456917, 26462399, 26473523, 26473769, 26473770, 26473771, 26473772, 26473773, 26473774, 26495372, 26495950, 26500637, 26500638, 26512452, 26512453, 26512454, 26512455, 26512456, 26512457, 26512458, 26512459, 26512480, 26512481, 26512483, 26512485, 26549972, 26552065, 26556788, 26556789, 26559542, 26559543, 26559544, 26559548, 26581407, 26581408, 26582103, 26582104, 26582105, 26582106, 26582107, 26588072, 26588073, 26588074, 26588075, 26588076, 26628443, 26628444, 26638830, 26638831, 26651713, 26651714, 26651715, 26651716, 26665561, 26665567, 26665571, 26665572, 26665573, 26685875, 26685876, 26685877, 26685878, 26685879, 26699192, 26699193, 26699194, 26699195, 26699196, 26699197, 26728782, 26728784, 26728785, 26759345, 26760530, 26778894, 26778895, 26778896, 26778897, 26778898, 26779080, 26779081, 26779082, 26779083, 26793782, 26793783, 26793784, 26808197, 26808198, 26808199, 26808300, 26808301, 26808302, 26808303, 26848720, 26848721, 26848722, 26848723, 26848724, 26848725, 26871168, 26871169, 26871170, 26871171, 26871172, 26871173, 26871174, 26910997, 26910998, 26910999, 26911840, 26911841, 26911842, 26911845, 26919040, 26919041, 26919042, 26960166, 26960167, 26960168, 26960169, 26960170, 26960171, 26960172, 26960173, 26960174, 26960175, 27009668, 27027289, 27027290, 27027291, 27027292, 27062054, 27062055, 27062056, 27062057, 27065830, 27065831, 27065832, 27065833, 27065834, 27065835, 27100017, 27100018, 27100019, 27100240, 27100241, 27100242, 27110096, 27110097, 27121582, 27121583, 27121584, 27121585, 27121620, 27121621, 27121625, 27148636, 27148637, 27148638, 27162326, 27162327, 27162328, 27162329, 27182896, 27182897, 27182898, 27182899, 27203768, 27203769, 27203770, 27203771, 27203772, 27203773, 27255217, 27255219, 27255220, 27255221, 27255222, 27255223, 27308422, 27308423, 27308424, 27308425, 27335091, 27335092, 27335093, 27335094, 27340629, 27340630, 27340632, 27340633, 27340634, 27340638, 27347592, 27347593, 27384705, 27384706, 27384713, 27384715. Exp. 05/10/2022 to 05/26/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 8MM 2CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545930

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
Batches: 25644951, 25649190, 25650286, 25651334, 25654287, 25947916, 25947918, 26010397, 26058298, 26406532, 26435581, 26449368, 26533973, 26555544, 26868194, 27074110, 27269956, 27384708. GTIN: 08714729283843 Exp. 05/27/2022 to 05/26/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 4MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545890

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
GTIN: 08714729283805 Lot Numbers: 25612668, 25649812, 25704208, 25771760, 25878552, 26000695, 26010387, 26058284, 26087172, 26087173, 26123181, 26324742, 26366746, 26406513, 26429808, 26499853, 26527374, 26573853, 26638827, 26651718, 26665448, 26893604, 27026984, 27074109, 27145234, 27162321, 27255235, 27306699. Exp. 05/19/2022 to 05/13/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 6MM 2CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN:M00545910

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
GTIN: 8714729283829 Batches: 25623385, 25678822, 25739151, 25771772, 25975774, 26010392, 26051928, 26087733, 26123186, 26175469, 26406521, 26429810, 26456904, 26579839, 26581406, 26601326, 26660957, 26793786, 26896864, 27026985, 27096335, 27226570, 27255234, 27400203. Exp. 05/23/2022 to 05/28/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 8MM 4CM -for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545940

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
Batches: 25608760, 25612672, 25649815, 25649818, 25649822, 25649823, 25649827, 25649828, 25649832, 25649833, 25678824, 25678828, 25678829, 25678833, 25678834, 25678838, 25680098, 25680099, 25704224, 25704225, 25704226, 25704227, 25704228, 25704229, 25739159, 25739160, 25739161, 25739162, 25739163, 25739164, 25739165, 25739166, 25739167, 25739168, 25788242, 25789369, 25789801, 25836093, 25836094, 25836095, 25836096, 25836097, 25836098, 25836099, 25836140, 25836141, 25836142, 25836143, 25836144, 25836145, 25878556, 25894780, 25894781, 25894782, 25916457, 25939485, 25939684, 25940126, 25940127, 25940131, 25947920, 25947921, 25975779, 25975780, 25975781, 25975782, 25975783, 25975784, 25975785, 25975786, 25975787, 26000581, 26000582, 26000583, 26000584, 26051925, 26051926, 26051927, 26058299, 26058420, 26058421, 26058422, 26058425, 26096221, 26096222, 26096223, 26099224, 26123192, 26123193, 26123194, 26123195, 26123196, 26123250, 26123251, 26175474, 26175475, 26175476, 26175477, 26175478, 26175479, 26175500, 26207992, 26207993, 26207994, 26207995, 26207996, 26207997, 26207998, 26238135, 26240374, 26240376, 26240377, 26240378, 26247258, 26247259, 26247280, 26247281, 26247282, 26247283, 26247284, 26247285, 26284144, 26284145, 26284146, 26284147, 26284148, 26284149, 26284150, 26284151, 26324756, 26324758, 26324760, 26324762, 26324764, 26324765, 26324767, 26350408, 26351999, 26356443, 26366758, 26366759, 26366760, 26366761, 26366762, 26366763, 26366764, 26366765, 26366766, 26395974, 26406533, 26406534, 26406535, 26406536, 26406537, 226435588, 26456918, 26456919, 26473775, 26473776, 26473777, 26473778, 26491312, 26491313, 26491314, 26491319, 26491480, 26512487, 26512488, 26512490, 26527375, 26527376, 26527377, 26527378, 26551465, 26551466, 26551467, 26551468, 26551470, 26577498, 26613121, 26614494, 26614495, 26614496, 26614497, 26614498, 26614800, 26614801, 26628445, 26628446, 26628447, 26651711, 26651712, 26665036, 26665037, 26665038, 26665039, 26665360, 26665361, 26696684, 26696685, 26696686, 26696687, 26706788, 26706789, 26706790, 26706791, 26706792, 26706793, 26706794, 26760454, 26760456, 26760458, 26760459, 26760520, 26760521, 26760522, 26760523, 26760524, 26760525, 26779085, 26799125, 26799126, 26799127, 26799128, 26799129, 26818882, 26818883, 26818884, 26818885, 26818886, 26818887, 26818888, 26818889, 26818890, 26818891, 26818892, 26848726, 26848727, 26848728, 26848729, 26848730, 26848731, 26888163, 26888164, 26888165, 26888166, 26888167, 26888168, 26910996, 26919048, 26919049, 26919050, 26919051, 26919341, 26990595, 26990596, 26990598, 26990599, 26990980, 26990981, 26990982, 27008813, 27008814, 27008815, 27008816, 27008817, 27009671, 27027284, 27027285, 27027286, 27027287, 27027288, 27055010, 27055018, 27062058, 27065836, 27065837, 27065838, 27065839, 27074113, 27074114, 27100243, 27100244, 27110098, 27110099, 27110720, 27121586, 27121587, 27121588, 27121589, 27148635, 27162330, 27162331, 27162332, 27183300, 27183301, 27183302, 27203774, 27203775, 27203776, 27203777, 27203778, 27203779, 27255225, 27255226, 27255227, 27255228, 27255229, 27255230, 27255231, 27255232, 27255233, 27265232, 27269957, 27269958, 27269959, 27308426, 27308427, 27335095, 27335096, 27335097, 27347594, 27347595, 27347596, 27384709, 27393786, 27407169, 27408779, 27408920, 274089216406538, 26426920, 26435582, 26435583, 26435585, 26435586, 26435587, 26435588, 26456918, 26456919, 26473775, 26473776, 26473777, 26473778, 26491312, 26491313, 26491314, 26491319, 26491480, 26512487, 26512488, 26512490, 26527375, 26527376, 26527377, 26527378, 26551465, 26551466, 26551467, 26551468, 26551470, 26577498, 26613121, 26614494, 26614495, 26614496, 26614497, 26614498, 26614800, 26614801, 26628445, 26628446, 26628447, 26651711, 26651712, 26665036, 26665037, 26665038, 26665039, 26665360, 26665361, 26696684, 26696685, 26696686, 26696687, 26706788, 26706789, 26706790, 26706791, 26706792, 26706793, 26706794, 26760454, 26760456, 26760458, 26760459, 26760520, 26760521, 26760522, 26760523, 26760524, 26760525, 26779085, 26799125, 26799126, 26799127, 26799128, 26799129, 26818882, 26818883, 26818884, 26818885, 26818886, 26818887, 26818888, 26818889, 26818890, 26818891, 26818892, 26848726, 26848727, 26848728, 26848729, 26848730, 26848731, 26888163, 26888164, 26888165, 26888166, 26888167, 26888168, 26910996, 26919048, 26919049, 26919050, 26919051, 26919341, 26990595, 26990596, 26990598, 26990599, 26990980, 26990981, 26990982, 27008813, 27008814, 27008815, 27008816, 27008817, 27009671, 27027284, 27027285, 27027286, 27027287, 27027288, 27055010, 27055018, 27062058, 27065836, 27065837, 27065838, 27065839, 27074113, 27074114, 27100243, 27100244, 27110098, 27110099, 27110720, 27121586, 27121587, 27121588, 27121589, 27148635, 27162330, 27162331, 27162332, 27183300, 27183301, 27183302, 27203774, 27203775, 27203776, 27203777, 27203778, 27203779, 27255225, 27255226, 27255227, 27255228, 27255229, 27255230, 27255231, 27255232, 27255233, 27265232, 27269957, 27269958, 27269959, 27… (truncated, 5190 characters total — see the official FDA record for the full value)
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

iDesign, Model - G300: System AWS (International), System AWS (China), Advanced WaveScan Studio (United States); iDesign Refractive Studio Aberrometer (International) and (United States), Model: G301

Aberrometer and precision laser systems are affected by a remote code execution vulnerability existing when the Microsoft Windows Print Spooler service is enabled, and improperly performs privileged file operations. This could be exploited to run arbitrary code with SYSTEM privileges, allowing for program installation; view/change/deleting data; or creation of new accounts with full user rights.

AKALARAZCACOCTDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKORPASCSDTNTXUTVAVTWAWI
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88986
Lot/product code:
G300 with Windows XP. G301 with Windows 7 Embedded System.
Recalling firm:
AMO Manufacturing USA, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

Catalys Precision Laser System, Models: Catalys-U (United States), Catalys-I (International), Catalys-C (China); and Catalys Precision Laser System No Bed, Models: 0160-6020 (United States), 0160-6010 (International)

Aberrometer and precision laser systems are affected by a remote code execution vulnerability existing when the Microsoft Windows Print Spooler service is enabled, and improperly performs privileged file operations. This could be exploited to run arbitrary code with SYSTEM privileges, allowing for program installation; view/change/deleting data; or creation of new accounts with full user rights.

AKALARAZCACOCTDEFLGAHIIAIDILINKSKYLAMAMDMEMIMNMOMSMTNCNDNENHNJNMNVNYOHOKORPASCSDTNTXUTVAVTWAWI
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88986
Lot/product code:
Catalys-U and Catalys-I with Windows 7 Ultimate/Professional/Embedded Standard. Catalys-C with Windows 7 Embedded Standard. 0160-6020 and 0160-6010 with Windows 7 Professional/Embedded Standard.
Recalling firm:
AMO Manufacturing USA, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 21, 2021

HURRICANE RX DILATION BALLOON 4MM 4CM-for endoscopic dilatation of strictures of the biliary tree and the Sphincter of Oddi. UPN: M00545900

Balloon pinhole results in losss pressure or fails to gain or maintain pressure, causing prolonged procedure

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FDA has not published a risk classification for this recall yet.

Recall #:
88991
Lot/product code:
GTIN: 08714729283812 Lot Numbers: 25576719, 25576720, 25576721, 25576769, 25611564, 25612669, 25612670, 25612671, 25612673, 25612674, 25623377, 25623378, 25623379, 25623380, 25623381, 25623382, 25623383, 25623384, 25640115, 25649813, 25649816, 25678821, 25678826, 25678831, 25678836, 25680096, 25704209, 25704210, 25704211, 25704212, 25704213, 25704214, 25704215, 25704216, 25739146, 25739147, 25739149, 25739150, 25771761, 25771762, 25771763, 25771764, 25771765, 25771766, 25771767, 25771768, 25771769, 25771770, 25771771, 25836081, 25836082, 25878553, 25878554, 25878555, 25894783, 25916270, 25916271, 25916445, 25916446, 25940122, 25940123, 25947675, 25947677, 25947678, 25947900, 25947902, 25947904, 25947905, 25975766, 25975767, 25975768, 25975769, 25975770, 25975771, 25975772, 25975773, 26000472, 26000473, 26000474, 26000475, 26000696, 26000697, 26000698, 26000699, 26010388, 26010389, 26010390, 26010391, 26058285, 26058286, 26087174, 26087175, 26087176, 26087177, 26087178, 26087179, 26087720, 26087721, 26087722, 26087723, 26087724, 26087725, 26087726, 26087727, 26087728, 26087729, 26087730, 26087731, 26087732, 26123182, 26123183, 26123184, 26123185, 26123244, 26123245, 26123246, 26175465, 26175466, 26175467, 26175468, 26207974, 26207975, 26207976, 26207977, 26207978, 26207979, 26207980, 26207981, 26207982, 26238131, 26240367, 26247246, 26247247, 26283625, 26283626, 26283627, 26283628, 26283629, 26283630, 26283631, 26324745, 26324747, 26344528, 26344529, 26348351, 26356445, 26366747, 26366748, 26366749, 26366750, 26366751, 26366752, 26406514, 26406515, 26406516, 26406517, 26406518, 26406519, 26406520, 26429809, 26435534, 26435535, 26435536, 26444430, 26447362, 26447363, 26449367, 26456914, 26456915, 26473765, 26473766, 26473767, 26473768, 26495948, 26499146, 26501878, 26511846, 26512444, 26512445, 26512446, 26512447, 26512448, 26512449, 26512450, 26512451, 26540309, 26556786, 26556787, 26559139, 26559540, 26559541, 26559546, 26559547, 26581401, 26581402, 26581403, 26581404, 26581405, 26582100, 26582101, 26582102, 26588068, 26588069, 26588070, 26588071, 26628440, 26628441, 26628442, 26638828, 26638829, 26651717, 26660956, 26665449, 26665450, 26665458, 26665560, 26677021, 26685872, 26685873, 26685874, 26699186, 26699187, 26699188, 26699189, 26699190, 26699191, 26728358, 26728359, 26728780, 26728781, 26769421, 26778891, 26778892, 26778893, 26792383, 26792384, 26792386, 26793780, 26793781, 26808194, 26808195, 26808196, 26818638, 26818639, 26818880, 26818881, 26848716, 26848717, 26848718, 26848719, 26872354, 26872355, 26872356, 26872357, 26872358, 26906626, 26906627, 26906628, 26906629, 26906630, 26906631, 26919043, 26919044, 26919045, 26919046, 26919047, 26940194, 26956470, 26956471, 26956472, 26956473, 26956474, 26956475, 26956476, 26956477, 26956478, 26956479, 27008818, 27008819, 27025671, 27027293, 27027294, 27027295, 27027296, 27027297, 27027298, 27027299, 27065828, 27065829, 27074111, 27074112, 27100015, 27100016, 27110095, 27121580, 27121581, 27121622, 27121623, 27121624, 27162322, 27162323, 27162324, 27162325, 27182893, 27182894, 27182895, 27183306, 27183307, 27183308, 27203712, 27203713, 27203714, 27203715, 27203716, 27203717, 27203718, 27203719, 27203760, 27203761, 27203762, 27203763, 27203764, 27203765, 27203766, 27203767, 27255211, 27255212, 27255213, 27255214, 27265231, 27269950, 27269951, 27269953, 27269954, 27269955, 27308420, 27308421, 27335099, 27335460, 27340626, 27340636, 27340637, 27347590, 27347591, 27384704, 27393782, 27408924 Exp. 05/10/2022 to 05/31/2023
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 22, 2021

The Ocean Water Seal Chest Drain is a plastic, three bottle vacuum collection device. It consists of a collection chamber that holds shed mediastinal blood, a water seal chamber using a water seal that prevents air from entering into the pleural space and a suction control chamber, which incorporates a mechanical regulator to control suction pressures imposed upon the patient's pleural cavity.

Inadequate/inappropriate Set-Up Instructions, which may result in delay in treatment and an unreasonable risk of harm to the patient

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FDA has not published a risk classification for this recall yet.

Recall #:
88923
Lot/product code:
Product Code/REF Number 2002-400; Lot codes: 441533, 443300, 443608, 443629, 444473, 445527, 448966, 449683, 450899, 450900, 451270, 451988, 452177, 452814, 454577, 455871, 458264, 458604, 459198, 459642, 462192, 462194, 464075, 464076, 465037, 466247, 469921, 470627, 471651,471703, 472562, 472785 and 473725.  UDI Code: 00650862100211
Recalling firm:
Atrium Medical Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 22, 2021

Abbott HeartMate Touch Communication System, REF: HMT1100 (US), HMT1100-R (Rental US), HMT1150 (EU)

If LVAS communication system is trying to establish Bluetooth connection and another Bluetooth-enabled device is nearby and advertising for Bluetooth connection, the Bluetooth connectivity interference may cause the system App to close or fail to open. Once Bluetooth adaptor is connected, barring disconnection, all functionality is unaffected; the device will continue to operate as expected.

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FDA has not published a risk classification for this recall yet.

Recall #:
88876
Lot/product code:
All serial numbers.
Recalling firm:
Thoratec Corp.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 26, 2021

The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range with an intended use of disinfecting surfaces.

Excessive ultraviolet-C radiation

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FDA has not published a risk classification for this recall yet.

Recall #:
89050
Lot/product code:
Safe-T Lite
Recalling firm:
MAX LUX CORP
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 28, 2021

OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control Console 2 REF 450-0021-01 -Power Control Console 2 REF ECOS-450-0021-00 -OsteoMed OsteoPower Power Console 2i REF 450-0005-00 -OsteoMed D-Power Control Console 2i REF 450-0005-01 -Power Control Console 2i REF ECOS-450-0005-00 OsteoMed Footswitches: -OsteoMed BMF Footswitch REF 450-0390 -D-Bi-Directional Master Footswitch REF 450-0380 -D-Uni-Directional Footswitch II REF 450-0350 -D-Bi-Directional Footswitch II REF 450-0360 -D-Uni-Directional Master Footswitch REF 450-0370

Due to consoles not in compliance with the latest electrical safety standards IEC 60601 and as a result shocked a patient.

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▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
88990
Lot/product code:
Product#/Brand Name/UDI Code: 450-0005-00 / OsteoMed OsteoPower Power Console 2i / 0084569401211 450-0021-00 / OsteoMed OsteoPower Power Console 2 / 0084569401215 450-0390 / OsteoMed BMF Footswitch / 0084569401215 450-0005-01 / OsteoMed D-Power Control Console 2i / 0084569401211 450-0021-01 / OsteoMed D-Power Control Console 2 / 0084569401211 ECOS-450-0021-00 / Power Control Console 2 / 0084569401211 ECOS-450-0005-00 / Power Control Console 2i / 0084569401211 Serial Numbers: 0332004 450-0005-01 0422006 450-0005-00 0423001 450-0005-01 0434003 S 0434004 S 0434010 S 0443004 0423005 450-0005-01 0449004s 0509004S 0509005S 0506027 0445003 0445005 9912003 0515009 0525014 0532001 0521042 0521045 0535006 0535007 0537031 0537032 0537033 0537034 0540005 0547022 0551022 0551025 0552008 0552009 0611004 0604070 0616001 0616002 0615005 0615009 0615010 0615039 0616003 0616005 0615041 0620004 0620005 0622022 0622023 0633024 0641004 0643068 0645002 0645003 0641009 0648023 0648025 0649002 0649003 0701004 0702021 0701005 0640004 0701006 0701009 0704036 0651097 0714001 0714002 0715029 0715031 0715032 0718003 0719005 0722041 0727024 0727025 0721005 0729044 0734030 0738015 0738017 0740001 0743032 0743033 0743034 0741013 0743036 0743037 0750022 0743038 0750023 0739022 0739023 0803016 0808001 0751032 0811002 0805025 0807056 0820004 0820004 0822030 0832057 0835005 0835004 0839048 0839048 0839049 0839049 0843053 0843054 0852046 0852002 0922072 0931001 0931003 0940011 0944016 0944006 0951020 0949001 1011002 1011003 1004051 1004052 1019002 1004054 1004055 1022048 1019005 1032001 1024002 1034007 1034008 1033010 1034009 1034010 1046013 1041033 1038009 1050036 1047020 1108032 1108033 1109006 1051004 1052014 1123010 1123012 1128022 1128023 1128026 1146012 1152006 0008006 9916005 1152007 1116005 1203041 1152008 1152009 1138003 1138005 1211003 9847002 1213003 1213004 1211005 1216001 1226008 1236044 1236040 1226007 1216002 1233042 1240054 1240055 1233041 1216005 1233045 1242003 1249002 1242004 1249003 1303005 1303002 1306002 1249005 1312002 1312003 1306004 1306005 1306001 0002001 1317012 0023005S 9916008 1240056 1317002 1317004 1336014 1340002 1340005 1341001 1341002 1346001 1346010 1346003 1349003 1349004 1341003 1349005 1351013 1346002 1405005 1405006 1420002 1420003 1405002 1417005 1424008 1424009 1424010 1417006 1434001 1434002 1434003 1434004 1441001 1441002 1441004 1445007 1445008 0244009 0720026 1509001 1509003 1516001 1516002 1518002 1521001 1521001 1521003 1521003 1528001 1528003 1528004 1528005 9942003 1533004 1533005 1528006 1537001 1537002 1537003 1539032 1539033 1539034 1547005 1547009 1543009 1553003 1543010 1604022 1604021 1614009 1134004 1614012 1614014 1604025 1604025 1610028 1610031 1610032 0603007 1410002 1620009 0232001 0548003 1622021 1604024 1610030 1622022 1622023 1622024 1638026 1634018 1634019 1638028 1638029 1634020 1634022 1638034 1638034 1634023 1634023 1634024 1634024 1634025 1634025 1639056 1639056 1639057 1639057 1639058 1644011 1644013 1643017 1644014 1644015 1644015 1643018 1651024 1651026 1644016 1651006 1707004 1707004 1707009 1707009 1651007 1651007 1710003 1710004 1651008 1651009 1651010 1651011 1712018 1710006 1710007 1711062 1711064 1711066 1711067 1715015 1651013 1711060 1711061 1715007 1715008 0751070 1719021 1719022 1719023 1711065 1713012 1721013 0651095 0051007S 1713013 1713014 1713015 1713016 1721015 1721016 1721017 1721018 1721019 1721014 1713017 1713018 1713019 1722009 1737018 1737017 1722011 1722012 1737019 1737020 1743001 1722013 1722014 1722015 1722016 1722017 1722018 1743009 1743007 1743008 1743010 1746027 1734014 1734015 1734016 1746031 1746030 1734017 1734018 1748010 1734019 1734020 1748009 1748001 1748003 1748006 1748007 1817052 1817053 1817054 1817055 1817056 1804002 1804010 1804001 1804003 1804004 1804005 1804007 1804006 1823017 1822008 1822010 1822014 1835012 1835013 1835020 1004053 1838001 1822015 1822016 1848001 1838003 1838004 1838005 1848002 1849017 1849019 1838006 1838007 1838008 1838009 1838010 1846025 1901001 1901002 1848003 1901003 1901004 1904003 1901009 1901010 1846026 1846027 1904001 1904002 1907011 1907012 1907013 1904004 1904005 1904006 1904007 1904008 1904009 1904010 1910031 1910032 1910033 1910034 1928046 1910035 1910036 1910037 1928047 1928048 1910039 1928049 1928050 1934001 1934002 1934003 1934004 1934005 1934006 1915001 1915002 1915003 1915004 1915005 1915006 1915007 1915008 1915009 1915010 1941001 1946002 1941002 1941003 1941004 1946003 1946004 1946005 2002034 1941005 2014016 2014017 2014018 2014019 2014020 1941006 2038001 2038002 1941007 1941008 2038003 2038004 2038005 2038006 2038007 2038008 1941009 2008002 2038009 2008003 2008004 2041001 0639018 2008005 2041002 2008001 2041003 2041006 2041007 2041008 2008007 2008008 2008009 2008010 2014001 2041009 2014002 2014003 2014004 ========================================================= -450-0380 / D-Bi-Directional Master Footswitch / 0084569401215 -450-0350 / D-Uni-Directional Footswitch II / 0084569401215 -450-0360 /… (truncated, 9865 characters total — see the official FDA record for the full value)
Recalling firm:
Osteomed, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled October 28, 2021

Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray device produces conventional 2D X-ray images and Xray projection images for the reconstruction of a 3D view. The device is operated and used by qualified healthcare professionals.

It was noticed in production on 28.10.2021, that the final testing database gives a pass result for Pan ADC repeatability test even when the test result is not within the set acceptance criteria (repeatability within 4%).

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FDA has not published a risk classification for this recall yet.

Recall #:
95017
Lot/product code:
DI: 06430035872725, 06430035872732, 06430035872749, 06430035872756, 06430035872763, 06430035872770
Recalling firm:
Palodex Group Oy
View official FDA record (opens in a new tab)