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Recalls affecting Wisconsin

Data last updated: September 9, 2026 at 1:18 PM UTC

16,929 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

▸Full report
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

▸Full report
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

▸Full report
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

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusE. coliAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

▸Full report
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

View FDA’s announcement (opens in a new tab)
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

▸Full report
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)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

▸Full report
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

View FDA’s announcement (opens in a new tab)
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)
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)
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

▸Full report
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 May 22, 2020

Fujifilm Synapse PACS Software Version 5.5.x and 5.7.x- intended as interface to the FUJIFILM Synapse PACS Software (Server)

Lateromedial (LM) and Lateromedial Oblique (LMO) Orientation Markers may be displayed incorrectly on the 3D TOMO slider bar. In addition, the slice location of the image and/or the slice direction could be incorrect as well, and result in misdiagnosis

ALL 50 STATES
▸Full report

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

Recall #:
85793
Lot/product code:
Serial Numbers: SY-01-00358350-11 SY-01-00048100 SY-01-01421950-151 SY-01-0080093778 SY-01-00745300 SY-01-0080087818 SY-01-00358350-16 SY-01-00544800 SY-01-01333000-34 SY-01-07012810 SY-01-0080082385 SY-01-0080078513 SY-01-07059500 SY-01-01333000-07 SY-01-01333000-20 SY-01-01333000-34 SY-01-07302600 SY-01-00127000 SY-01-07038976 SY-01-01487000-02 SY-01-00272120 SY-01-00349940 SY-01-00233520 SY-01-0080087409 SY-01-00233710 SY-01-00358350-03 SY-01-00236550 SY-01-0052282 SY-01-00254800-02 SY-01-000254800 SY-01-00269450 SY-01-07039120-01 SY-01-00272350-01 SY-01-00272410 SY-01-00106300 SY-01-00316710 SY-01-00277570-04 SY-01-00322350 SY-01-00322360 SY-01-07055566 SY-01-00493810-327 SY-01-01487000-01 SY-01-07060430-01 SY-01-80096794 SY-01-0079187 SY-01-09003000 SY-01-00465550 SY-01-00493810-112 SY-02-01138010-47 SY-01-00463100 SY-01-00493810-340 SY-01-0080092404 SY-01-00586560 SY-01-00591100 SY-01-00593500-01 SY-01-0080076025 SY-01-01447400-01 SY-01-00493810-155 SY-01-07127057 SY-0180097541 SY-01-00605610 SY-01-00616700-02 SY-01-0080053255 SY-01-0080080176 SY-01-00658580-01 SY-01-00228750-01 SY-01-01687500 SY-01-0080057825 SY-01-00693860 SY-01-0080071248 SY-01-00798760 SY-01-00804700-01 SY-01-0074955 SY-01-0080055290 SY-01-0080074389 SY-01-07160281 SY-01-0077489 SY-01-00873500 SY-01-07163410 SY-0080053050-001 SY-01-00103613 SY-01-00899150 SY-01-00816310 SY-01-0080094741 SY-01-07182322 SY-01-00971200 SY-01-0080092600 SY-01-80097226 SY-01-01034770 SY-01-09625000 SY-01-01072260 SY-01-01446300 SY-01-00769050-01 SY-01-01079071 SY-01-00493810-137 SY-01-00439700-10 SY-02-00858500 SY-01-07274900-01 SY-01-00493810-157 SY-01-01421950-26 SY-01-01134010 SY-01-00082610 SY-01-07242000 SY-01-00493810-300 SY-01-00949090 SY-01-00493810-97 SY-01-0080073752 SY-01-00322221 SY-01-05050280-60 SY-01-08131000 SY-01-01255600-03 SY-01-01272111 SY-01-07264334 SY-01-01401510-02 SY-01-80060398 SY-01-00493810-54 SY-01-01430700 SY-01-01447400 SY-01-01451260 SY-01-01318310 SY-01-00529515 SY-01-01327350 SY-01-01482450 SY-01-01489350 SY-01-01558860 SY-01-01573510 SY-01-00822790 SY-01-0080087769 SY-03-00070210 SY-01-07214790 SY-01-01717500-15 SY-01-00398300-10 SY-01-0080072627 SY-01-0080055858 SY-01-0080055213
Recalling firm:
Fujifilm Medical Systems U.S.A., Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 26, 2020

RayStation standalone software treatment planning system (RayStation 8A, 8B, 9A, and 9B, including all service packs) model no. 8.0, 8.1, 9.0, 9.1, 9.2

It is not obvious that the manual import of a treatment record into RayCare PACS does not automatically import the same data into RayTreat. In addition, there is an issue found with the display of planned and recorded Gantry Angle in the delivered beam list in RayTreat.

ALL 50 STATES
▸Full report

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

Recall #:
85796
Lot/product code:
Software versions 8.0.0.61 , 8.0.1.10 , 8.1.0.47 , 8.1.1.8 , 8.1.2.5 , 9.0.0.113 , 9.1.0.933 and 9.2.0.483
Recalling firm:
RAYSEARCH LABORATORIES AB
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 27, 2020

Metformin Hydrochloride Extended-Release Tablets, USP 500 mg, 100 count bottles, Rx Only Manufactured by: Apotex, Inc. Toronto, Ontario Canada M9L 1T9 Manufactured for: Apotex Corp. Weston, Florida 33326 NDC 60505-0260-1

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above acceptable intake levels

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1303-2020
Lot/product code:
All lots remaining within expiry
Recalling firm:
Apotex Inc.
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, Bulk, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-BULK

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1350-2020
Lot/product code:
HA01320A 1/31/2021 HA01420A 1/31/2021 HA06820A 1/31/2021 HB03620A 1/31/2021 HB03720A 1/31/2021 HB03820A 1/31/2021 HB03920A 1/31/2021 HB04020A 1/31/2021 HB04120A 1/31/2021 HB04220A 1/31/2021 HB04320A 2/28/2021 HB04420A 1/31/2021 HB04520A 2/28/2021 HB05020A 2/28/2021 HB05120A 2/28/2021 HB05220A 2/28/2021 HB05320A 2/28/2021 HB05420A 2/28/2021 HB05520A 2/28/2021 HB05620A 2/28/2021 HB07020A 2/28/2021 HB07120A 2/28/2021 HB07220A 2/28/2021 HB07320A 2/28/2021 HB07520A 2/28/2021 HB07620A 2/28/2021 HB07720A 2/28/2021 HB07820A 2/28/2021 HB07920A 2/28/2021 HB08020A 2/28/2021 HB08220A 2/28/2021 HF05519A 6/30/2020 HF05619A 6/30/2020 HF05719A 6/30/2020 HF05819A 6/30/2020 HF05919A 6/30/2020 HF06019A 6/30/2020 HF06119A 6/30/2020 HF06219A 6/30/2020 HF06319A 6/30/2020 HF07719A 6/30/2020 HF07819A 6/30/2020 HF07919A 6/30/2020 HF08019A 6/30/2020 HF08119A 6/30/2020 HF08219A 6/30/2020 HF08319A 6/30/2020 HF08419A 6/30/2020 HF08519A 6/30/2020 HF08619A 6/30/2020 HF10119A 6/30/2020 HF10219A 6/30/2020 HF10319A 6/30/2020 HF10419A 6/30/2020 HF10519A 6/30/2020 HF10619A 6/30/2020 HF10719A 6/30/2020 HF10819A 6/30/2020 HF10919A 6/30/2020 HF11019A 6/30/2020 HF11119A 6/30/2020 HG07219A 7/31/2020 HG07319A 7/31/2020 HG07419A 7/31/2020 HG07519A 7/31/2020 HG07619A 7/31/2020 HG07719A 7/31/2020 HG07819A 7/31/2020 HG07919A 7/31/2020 HG08019A 7/31/2020 HG08119A 7/31/2020 HH00619A 7/31/2020 HH00719A 7/31/2020 HH00819A 7/31/2020 HH00919A 7/31/2020 HH01019A 7/31/2020 HH01119A 8/31/2020 HH01219A 8/31/2020 HH01319A 8/31/2020 HH01419A 8/31/2020 HH01519A 8/31/2020 HH07319A 8/31/2020 HH07419A 8/31/2020 HH07519A 8/31/2020 HH07619A 8/31/2020 HH07719A 8/31/2020 HH07819A 8/31/2020 HH07919A 8/31/2020 HH08019A 8/31/2020 HH08119A 8/31/2020 HH08219A 8/31/2020 HH11119A 10/31/2020 HH11219A 10/31/2020 HH11319A 10/31/2020 HH11419A 10/31/2020 HH11519A 10/31/2020 HH11619A 10/31/2020 HH11719A 10/31/2020 HH11819A 10/31/2020 HH11919A 10/31/2020 HH12019A 10/31/2020 HH12119A 10/31/2020 HH12219A 10/31/2020 HH12319A 10/31/2020 HH12419A 10/31/2020 HH12519A 10/31/2020 HH12619A 10/31/2020 HH12719A 10/31/2020 HH12819A 10/31/2020 HH12919A 10/31/2020 HH13019A 10/31/2020 HL00119A 10/31/2020 HL00219A 11/30/2020 HL00319A 11/30/2020 HL00419A 11/30/2020 HL00519A 11/30/2020 HL00619A 11/30/2020 HL00719A 11/30/2020 HL00819A 11/30/2020 HL00919A 11/30/2020 HL01019A 11/30/2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg, Rx only, 100 Tablets bottles, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad, 388213, INDIA Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 65162-179-10

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1349-2020
Lot/product code:
AM181337A 10/31/2020 AM181338A 10/31/2020 AM181339A 11/30/2020 AM181340A 11/30/2020 AM181341A 11/30/2020 AM181342A 11/30/2020 AM181343A 11/30/2020 AM181344A 11/30/2020 AM181356A 11/30/2020 AM181357A 11/30/2020 AM181358A 11/30/2020 AM181359A 11/30/2020 AM181360A 11/30/2020 AM181361A 11/30/2020 AM181362A 11/30/2020 AM181363A 11/30/2020 AM181415A 11/30/2020 AM190040B 12/31/2020 AM190041A 12/31/2020 AM190042A 12/31/2020 AM190043A 12/31/2020 AM190044A 12/31/2020 AM190045A 12/31/2020 AM190046A 12/31/2020 AM190473B 4/30/2021 AM190474A 4/30/2021 AM190475A 4/30/2021 AM190476A 4/30/2021 AM190477A 4/30/2021 AM190478A 4/30/2021 AM190479A 4/30/2021 AM190480A 4/30/2021 AM190481A 4/30/2021 AM190482A 4/30/2021 AM190834A 7/31/2021 AM190835A 7/31/2021 AM190836A 7/31/2021 AM190837A 7/31/2021 AM190838A 7/31/2021 AM191004A 8/31/2021 AM191005A 8/31/2021 AM191006A 8/31/2021 AM191007A 8/31/2021 AM191008A 9/30/2021 AM191271A 10/31/2021 AM191272A 10/31/2021 AM191273A 10/31/2021 AM191274A 10/31/2021 AM191338A 11/30/2021 AM191339A 11/30/2021 AM191340A 11/30/2021 AM191341 12/31/2021 AM191342 12/31/2021 AM200109 12/31/2021 AM200110 12/31/2021 AM200111 12/31/2021
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-release Tablets, USP 500 mg Rx Only 90 Tablets bottles, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad, 388213, INDIA Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08907 NDC 65162-178-09

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1344-2020
Lot/product code:
AM190123A 1/31/2021 AM190193A 1/31/2021 AM190194A 1/31/2021 AM190195A 1/31/2021 AM190196A 1/31/2021 AM190197A 1/31/2021 AM190198A 1/31/2021 AM190199A 1/31/2021 AM190200A 2/28/2021 AM190201A 2/28/2021 AM190202A 2/28/2021 AM190269A 2/28/2021 AM190270A 2/28/2021 AM190271A 2/28/2021 AM190272A 2/28/2021 AM190289A 2/28/2021 AM190290A 2/28/2021 AM190291A 2/28/2021 AM190292A 2/28/2021 AM190293A 2/28/2021 AM190294A 2/28/2021 AM190549A 4/30/2021 AM190550A 4/30/2021 AM190551A 4/30/2021 AM190552A 4/30/2021 AM190553A 4/30/2021 AM190554A 4/30/2021 AM190555A 5/31/2021 AM190556A 5/31/2021 AM190586A 5/31/2021 AM190587A 5/31/2021 AM190588A 5/31/2021 AM190589A 5/31/2021 AM190590A 5/31/2021 AM190605A 5/31/2021 AM190673A 6/30/2021 AM190707A 6/30/2021 AM190708A 6/30/2021 AM190709A 6/30/2021 AM190710A 6/30/2021 AM190714C 6/30/2021 AM190751C 6/30/2021 AM190752C 6/30/2021 AM190753A 8/31/2021 AM190754A 8/31/2021 AM190755A 8/31/2021 AM190756A 8/31/2021 AM190757A 8/31/2021 AM190929A 8/31/2021 AM190930A 8/31/2021 AM190931A 8/31/2021 AM190932A 8/31/2021 AM190933A 8/31/2021 AM190995A 8/31/2021 AM191000A 8/31/2021 AM191001A 8/31/2021 AM191002A 8/31/2021 AM191003A 8/31/2021 AM191034A 9/30/2021 AM191035A 9/30/2021 AM191036A 9/30/2021 AM191037A 9/30/2021 AM191038A 9/30/2021 AM191039A 9/30/2021 AM191086A 9/30/2021
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 1000 tablets bottles, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-10

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1352-2020
Lot/product code:
HF08618A 6/30/2020 HF08718A 6/30/2020 HF15418A 7/31/2020 HF15518A 7/31/2020 HH11818A 9/30/2020 HJ00818A 9/30/2020 HJ00918A 9/30/2020 HJ01018A 9/30/2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg Rx only 100 Tablets bottles, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0179-01

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1348-2020
Lot/product code:
HF02318A 6/30/2020 HF02418A 6/30/2020 HF02518A 6/30/2020 HF07718A 6/30/2020 HH02118A 7/31/2020 HM04418A 12/31/2020 HM04518A 12/31/2020 HM04618A 12/31/2020 HM04718A 12/31/2020 HM05518A 12/31/2020 HM05618A 12/31/2020 HM05718A 12/31/2020 HM05818A 12/31/2020 HM05918A 12/31/2020 HM06018A 12/31/2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, Rx Only, 100 count bottles, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-01

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1343-2020
Lot/product code:
HA07419A 1/31/2021 HB00119A 1/31/2021 HB00219A 1/31/2021 HB00319A 1/31/2021; HB00419A 2/28/2021 HB00519A 2/28/2021 HB00619A 2/28/2021 HB00719A 2/28/2021 HB00819A 2/28/2021 HB00919A 2/28/2021 HB01019A 2/28/2021 HB05119A 2/28/2021 HB05219A 2/28/2021 HB05319A 2/28/2021 HB05419A 2/28/2021 HB05519A 2/28/2021 HB09519A 2/28/2021 HB09619A 2/28/2021 HB09719A 2/28/2021 HB09819A 2/28/2021 HB09919A 2/28/2021; HC08219A 3/31/2021 HC08319A 3/31/2021 HC08419A 3/31/2021 HC08519A 3/31/2021 HC09019A 3/31/2021 HC09119A 3/31/2021 HC09219A 3/31/2021 HC09319A 3/31/2021 HC09419A 3/31/2021; HD03419B 4/30/2021 HD03519B 4/30/2021 HD03619B 4/30/2021 HD03719B 4/30/2021 HD03819B 4/30/2021 HD03919B 4/30/2021 HD04019B 4/30/2021 HD04119B 4/30/2021 HD04219A 4/30/2021 HD05819A 4/30/2021 HD05919A 4/30/2021 HD06019A 4/30/2021 HD06119A 4/30/2021 HD06219A 4/30/2021 HD06319A 4/30/2021 HD06419A 4/30/2021 HD09019A 4/30/2021 HD09119A 4/30/2021 HD09219A 4/30/2021 HE01219B 4/30/2021 HE01319B 4/30/2021 HE01419B 4/30/2021 HE01519B 4/30/2021; HE01619A 5/31/2021 HE01719A 5/31/2021 HE01819A 5/31/2021 HE04419A 5/31/2021 HE04519A 5/31/2021 HE04619A 5/31/2021 HE04719A 5/31/2021 HE04819A 5/31/2021 HE04919A 5/31/2021 HE05019A 5/31/2021 HE05119A 5/31/2021 HE05219A 5/31/2021 HE05319A 5/31/2021 HE07219A 5/31/2021 HE07319A 5/31/2021 HE07419A 5/31/2021 HE07519A 5/31/2021 HE07619A 5/31/2021 HF02219A 5/31/2021 HF02319A 5/31/2021; HF02419A 6/30/2021 HF02519A 6/30/2021 HF02619A 6/30/2021 HF02719A 6/30/2021 HF02819A 6/30/2021 HF02919A 6/30/2021 HF03019A 6/30/2021 HF03119A 6/30/2021 HF03219A 6/30/2021 HF03319A 6/30/2021 HF05419A 6/30/2021; HF03918A 6/30/2020 HF04018A 6/30/2020 HF04118A 6/30/2020 HF04218A 6/30/2020 HF04318A 6/30/2020 HF04418A 6/30/2020 HF06518A 6/30/2020 HF06818B 6/30/2020 HF06918B 6/30/2020 HF07018B 6/30/2020 HF07118B 6/30/2020 HF07218A 6/30/2020 HF07318A 6/30/2020 HF07418A 6/30/2020 HF08318A 6/30/2020 HF08418A 6/30/2020 HF08518A 6/30/2020; HF11219A 6/30/2021 HF11319A 6/30/2021 HF11419A 6/30/2021 HF11519A 6/30/2021 HF11619A 6/30/2021 HF11719A 6/30/2021 HF11819A 6/30/2021 HF11919A 6/30/2021 HF12019A 6/30/2021 HG00719A 6/30/2021 HG00819A 6/30/2021 HG00919A 6/30/2021 HG01019A 6/30/2021 HG01119A 6/30/2021 HG01219A 6/30/2021 HG01319A 6/30/2021 HG01419A 6/30/2021; HG01519A 7/31/2021 HG01619A 7/31/2021 HG02919A 7/31/2021 HG03019A 7/31/2021 HG03119A 7/31/2021 HG03219A 7/31/2021 HG03319A 7/31/2021 HG03419A 7/31/2021 HG03519A 7/31/2021 HG03619A 7/31/2021 HG03719A 7/31/2021 HG03819A 7/31/2021; HH08218A 8/31/2020 HH08318A 8/31/2020 HH08418A 8/31/2020 HH08518A 8/31/2020 HH08618A 8/31/2020 HH08718A 8/31/2020 HH08818A 8/31/2020 HH08918A 8/31/2020 HH09018A 8/31/2020 HH09118A 8/31/2020 HH09218A 8/31/2020 HH09318A 8/31/2020 HH09418A 8/31/2020 HH09518A 8/31/2020 HH09618A 8/31/2020 HH11218A 8/31/2020 HH11318A 8/31/2020 HH11418A 8/31/2020 HH11518A 8/31/2020; HH11618A 9/30/2020 HH11718A 9/30/2020 HJ04818A 9/30/2020 HJ04918A 9/30/2020 HJ08518A 9/30/2020; HJ08618A 10/31/2020 HJ08718A 10/31/2020 HJ08818A 10/31/2020 HJ08918A 10/31/2020 HJ09018A 10/31/2020 HJ09118A 10/31/2020 HK03718A 10/31/2020 HK03818A 10/31/2020 HK03918A 10/31/2020 HK04018A 10/31/2020 HK04118A 10/31/2020 HK04218A 10/31/2020 HK04318A 10/31/2020 HK04418A 10/31/2020 HK04518A 10/31/2020 HK04618A 10/31/2020 HK09318A 10/31/2020 HK09418A 10/31/2020 HK09518A 10/31/2020 HK09618A 10/31/2020 HK09718A 10/31/2020; HM00218A 12/31/2020 HM00318A 12/31/2020 HM00418A 12/31/2020 HM00518A 12/31/2020 HM00618B 12/31/2020 HM00718B 12/31/2020 HM00818B 12/31/2020 HM00918B 12/31/2020 HM01018B 12/31/2020; HM02918A 1/31/2021 HM03018A 1/31/2021 HM03218A 1/31/2021 HM03318A 1/31/2021 HM03418A 1/31/2021 HM03518A 1/31/2021 HM03618A 1/31/2021 HM03718A 1/31/2021 HM03818A 1/31/2021
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 90 count bottle, Rx Only, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-90

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1393-2020
Lot/product code:
HB10019A 03-2021 HB10119A 03-2021 HB10219A 03-2021 HB10319A 03-2021 HD02119A 04-2021 HD03319A 04-2021 HF09118A 06-2020 HF11618A 06-2020 HF15218A 07-2020 HF15318A 07-2020 HJ01418A 09-2020 HJ01518A 09-2020 HJ01618A 09-2020 HJ01718A 09-2020 HJ04718A 09-2020 HK03218A 10-2020 HK03318A 10-2020 HK03418A 10-2020 HK03518A 10-2020 HK03618A 10-2020 HK13718A 11-2020 HK13818A 11-2020 HK13918A 11-2020 HK14018A 11-2020 HK14118A 11-2020 HK14218A 11-2020 HK14318A 11-2020 HK14418A 11-2020 HK14518A 11-2020 HM00118A 11-2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg, 1000 tablets bottles, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad, 388213, INDIA Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 65162-0178-11

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1353-2020
Lot/product code:
HF08618A 6/30/2020 HF08718A 6/30/2020 HF15418A 7/31/2020 HF15518A 7/31/2020 HH11818A 9/30/2020 HJ00818A 9/30/2020 HJ00918A 9/30/2020 HJ01018A 9/30/2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, USP, Bulk, Rx Only, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0179-BULK

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1354-2020
Lot/product code:
HA01520A 1/31/2021 HA01620A 1/31/2021 HG01719A 7/31/2020 HG01819A 7/31/2020 HH09319A 8/31/2020 HH09419A 9/30/2020 HK07619A 10/31/2020 HK07719A 10/31/2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-release Tablets, USP, 500 mg Rx only, 100 Tablets bottles, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad 382213 India Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 65162-178-10

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1347-2020
Lot/product code:
AM181118AA 10/31/2020 AM181191AA 9/30/2020 AM181192AA 9/30/2020 AM181235AA 9/30/2020 AM181236AA 9/30/2020 AM181237AA 9/30/2020 AM181240AA 9/30/2020 AM181241AA 9/30/2020 AM181242AA 9/30/2020 AM181243AA 9/30/2020 AM181244AA 10/31/2020 AM181268AA 10/31/2020 AM181269AA 10/31/2020 AM181270AA 10/30/2020 AM181271AA 10/31/2020 AM181272AA 10/31/2020 AM181273AA 10/31/2020 AM181274AA 10/31/2020 AM181275AA 10/31/2020 AM181276AA 10/31/2020 AM181277AA 10/31/2020 AM181307AA 10/31/2020 AM181308AA 10/31/2020 AM181309AA 10/31/2020 AM181310AA 10/31/2020 AM181311AA 10/31/2020 AM181313AA 10/31/2020 AM181314AA 10/31/2020 AM181315AA 11/30/2020 AM181316AA 11/30/2020 AM181317AA 12/31/2020 AM181419AA 11/30/2020 AM181420AA 11/30/2020 AM181421AA 11/30/2020 AM181422AA 11/30/2020 AM181423AA 11/30/2020 AM181424AA 11/30/2020 AM181425AA 11/30/2020 AM181430BA 12/31/2020 AM181455AA 12/31/2020 AM181456AA 12/31/2020 AM181457AA 12/31/2020 AM181458AA 12/31/2020 AM181459AA 12/31/2020 AM181460AA 12/31/2020 AM181461AA 12/31/2020 AM181462AA 12/31/2020 AM181463AA 12/31/2020 AM181464AA 12/31/2020 AM181465AA 12/31/2020 AM190054AA 12/31/2020 AM190055AA 12/31/2020 AM190057AA 12/31/2020 AM190058AA 12/31/2020 AM190102AA 12/31/2020 AM190103AA 12/31/2020 AM190104AA 12/31/2020 AM190105AA 12/31/2020 AM190106AA 12/31/2020 AM190107AA 12/31/2020 AM190108AA 12/31/2020 AM190120AA 12/31/2020 AM190633AA 5/31/2021 AM190634AA 5/31/2021 AM190635AA 5/31/2021 AM190636AA 5/31/2021 AM190637AA 5/31/2021 AM190638AA 5/31/2021 AM190640AA 5/31/2021 AM190641AA 5/31/2021 AM190642AA 5/31/2021 AM190664AA 5/31/2021 AM190665AA 5/31/2021 AM190666AA 5/31/2021 AM190667AA 5/31/2021 AM190668AA 5/31/2021 AM190669AA 6/30/2021 AM190670AA 6/30/2021 AM190671AA 6/30/2021 AM190672AA 6/30/2021 AM190714AA 6/30/2021 AM190934A 8/31/2021 AM190991A 8/31/2021 AM190992A 8/31/2021 AM190993A 8/31/2021 AM190994A 8/31/2021 AM191040A 9/30/2021 AM191041A 9/30/2021 AM191083A 9/30/2021 AM191084A 9/30/2021 AM191085A 9/30/2021 AM191091A 9/30/2021 AM191092A 9/30/2021 AM191105A 9/30/2021 AM191106A 10/31/2021 AM191107A 10/31/2021 AM191109A 10/31/2021 AM191186A 10/31/2021 AM191187A 10/31/2021 AM191188A 10/31/2021 AM191189A 10/31/2021 AM191190A 10/31/2021 AM191191A 10/31/2021 AM191192A 10/31/2021 AM191193A 10/31/2021 AM191194A 10/31/2021 AM191195A 10/31/2021 AM191244A 10/31/2021 AM191245A 10/31/2021 AM191246A 10/31/2021 AM191247A 10/31/2021 AM191294A 11/30/2021 AM191295A 11/30/2021 AM191296A 11/30/2021 AM191365A 11/30/2021 AM191366A 11/30/2021 AM191367A 11/30/2021 AM191392A 11/30/2021 AM191393A 11/30/2021 AM191394A 11/30/2021 AM191395A 12/31/2021 AM200001A 12/31/2021 AM200002A 12/31/2021 AM200003A 12/31/2021 AM200004A 12/31/2021 AM200005A 12/31/2021 AM200006A 12/31/2021 AM200045A 12/31/2021 AM200046A 12/31/2021 AM200047A 12/31/2021 AM200048A 12/31/2021 AM200049A 12/31/2021 AM200050A 12/31/2021 AM200051A 12/31/2021 AM200052A 12/31/2021 AM200053A 12/31/2021 AM200081A 12/31/2021 AM200082A 12/31/2021 AM200083 12/31/2021 AM200087A 12/31/2021 AM200088A 12/31/2021 AM200089 12/31/2021 AM200090 12/31/2021 AM200091 12/31/2021 AM200100 1/31/2022 AM200101 1/31/2022 AM200102 1/31/2022 AM200138 1/31/2022 AM200139 1/31/2022 AM200140 1/31/2022 AM200141 1/31/2022 AM200142 1/31/2022 AM200143 1/31/2022 AM200144 1/31/2022 AM200193 1/31/2022 AM200194 1/31/2022 AM200195 1/31/2022 AM200196 1/31/2022 AM200197 1/31/2022 AM200198 1/31/2022 AM200199 1/31/2022 AM200200 1/31/2022 AM200202 1/31/2022 AM200203 1/31/2022 AM200204 1/31/2022 AM200205 1/31/2022 AM200206 1/31/2022 AM200207 1/31/2022 AM200208 1/31/2022 AM200209 1/31/2022 AM200210 1/31/2022 AM200211 1/31/2022 AM200284 2/28/2022 AM200285 2/28/2022 AM200287 2/28/2022 AM200288 2/28/2022 AM200289 2/28/2022 AM200290 2/28/2022 AM200291 2/28/2022 AM200292 2/28/2022
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-Release Tablets, 500 mg USP, 500 tablets bottles, Rx only, Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 53746-0178-05

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1351-2020
Lot/product code:
HF06618A 6/30/2020 HF06718A 6/30/2020
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 29, 2020

amneal Metformin Hydrochloride Extended-release Tablets, USP, 500 mg Rx Only, 500 Tablets bottles, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad 388213, INDIA Distributed by: Amneal Pharmaceuticals LLC Bridgewater, NJ 08807 NDC 65162-178-50

CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA) impurity above the acceptable intake level

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-1345-2020
Lot/product code:
AM180641A 6/30/2020 AM180642A 6/30/2020 AM180643A 6/30/2020 AM180644A 6/30/2020 AM180645A 6/30/2020 AM180646A 6/30/2020 AM180647A 6/30/2020 AM180880A 7/31/2020 AM180881A 7/31/2020 AM180882A 7/31/2020 AM180883A 7/31/2020 AM180884A 7/31/2020 AM180885A 7/31/2020 AM180886A 7/31/2020 AM180887A 7/31/2020 AM180888A 7/31/2020 AM180889A 7/31/2020 AM180936A 7/31/2020 AM180937A 7/31/2020 AM180938A 7/31/2020 AM180939A 7/31/2020 AM180940A 7/31/2020 AM180960A 7/31/2020 AM180961A 7/31/2020 AM180962A 7/31/2020 AM180963A 7/31/2020 AM180964A 7/31/2020 AM180965A 7/31/2020 AM180992A 7/31/2020 AM180993A 7/31/2020 AM180994A 8/31/2020 AM180995A 8/31/2020 AM180996A 8/31/2020 AM180997A 8/31/2020 AM181037A 8/31/2020 AM181038A 8/31/2020 AM181039A 8/31/2020 AM181040A 8/31/2020 AM181041A 8/31/2020 AM181079A 8/31/2020 AM181080A 8/31/2020 AM181081A 8/31/2020 AM181082A 8/31/2020 AM181083A 8/31/2020 AM181084A 8/31/2020 AM181085A 8/31/2020 AM181086A 8/31/2020 AM181087A 8/31/2020 AM181088A 8/31/2020 AM181089A 8/31/2020 AM181093A 8/31/2020 AM181094A 8/31/2020 AM181095A 8/31/2020 AM181096A 8/31/2020 AM181097A 8/31/2020 AM181098A 8/31/2020 AM181099A 8/31/2020 AM181100A 8/31/2020 AM181101A 8/31/2020 AM181102A 8/31/2020 AM181116A 8/31/2020 AM181117A 9/30/2020 AM181129A 8/31/2020 AM181130A 8/31/2020 AM181131A 8/31/2020 AM181132A 8/31/2020 AM181133A 9/30/2020 AM181134A 9/30/2020 AM181135A 9/30/2020 AM181136A 9/30/2020 AM181137A 9/30/2020 AM181138A 9/30/2020 AM181183A 9/30/2020 AM181184A 9/30/2020 AM181185A 9/30/2020 AM181186A 9/30/2020 AM181187A 9/30/2020 AM181188A 9/30/2020 AM181189A 9/30/2020 AM181190A 9/30/2020 AM181235A 9/30/2020 AM181236A 9/30/2020 AM181237A 9/30/2020 AM181238A 9/30/2020 AM181239A 9/30/2020 AM181240A 9/30/2020 AM181242A 9/30/2020 AM181243A 9/30/2020 AM181314A 10/31/2020 AM181315A 11/30/2020 AM190121B 12/31/2020 AM190122B 12/31/2020 AM190713AA 6/30/2021 AM191248A 10/31/2021 AM191249A 10/31/2021 AM200192 1/31/2022 AM200322A 2/28/2022
Recalling firm:
Amneal Pharmaceuticals of New York, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 2, 2020

Flow Coupler Monitor, GEM, Global Excellence Microsurgery, Rx Only

A firmware issue may cause the GEM1020M-2 Flow Coupler Monitor to intermittently shut down when a WiFi connection is not established.

AZCADCFLGAINLAMAMDMIMNMSNYPASCTXVAWAWI
▸Full report

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

Recall #:
85782
Lot/product code:
Product Code: 5156-00000-011, All Serial numbers
Recalling firm:
Baxter Healthcare Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 3, 2020

HYGENIC Winged Fiesta Kit, Model no. H02778 - Product Usage: The dental dam forceps are intended to be used in conjunction with the rubber dental dam and the dental dam clamps. The forceps are used to place and remove the dental dam clamps from the rubber dental dam.

Multiple Coltene batches of the product have a pin size larger than acceptable, which may make it difficult for the forceps to fit appropriately with dental dam clamps.

ALL 50 STATES
▸Full report

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

Recall #:
85794
Lot/product code:
Batch numbers:  J38382   J28715   J24868   J28716   J33647   J43944  J50980   J47108   J57802   J57061   J67133   J74174   J68563  J72691   If a distributor or end user received one of the batches listed above, they need to look at the batch number laser marked on the forceps themselves. If the forceps has any of the following batch numbers laser marked on them and the forceps do not fit with the dental dam clamps, the forceps should be returned to Coltene. Laser marked batch number:  1903 1904 1906 1907 1909 1910 1911 1915 1920 1921 1923 1927 1928 1930 1934 1940
Recalling firm:
Coltene Whaledent Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 3, 2020

PrimeStore Molecular Transport Medium (PS-MTM), Model Numbers LH-1-2, LH-1-3, LH-1-4, LH-1-5, LH-1-5CC, LH-1-15CC - Product Usage: intended for stabilization, transportation, and inactivation of infectious unprocessed nasal washes, nasopharyngeal, oral/throat swabs* suspected of containing Influenza A virus RNA. PS-MTM is also intended for the stabilization, transportation, and inactivation of infectious unprocessed sputum samples suspected of containing Mycobacterium tuberculosis (MTB) DNA from human samples.

The tubes may have been delivered to some users without labels. Users may not be able to identify the tubes without these labels. If samples stored or transported in tubes are tested on certain systems or come into contact with bleach they can produce cyanide gas. The solution in these tubes contains guanidine thiocynate and may put laboratory personnel at risk of exposure to cyanide gas when it comes into contact with bleach or reagents containing bleach.

ALL 50 STATES
▸Full report

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

Recall #:
86189
Lot/product code:
Lot Numbers: 200421A 200421B E200427A E200427B E2000505B CN200423 CN200427
Recalling firm:
LONGHORN VACCINES AND DIAGNOSTIC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 3, 2020

HYGENIC Simple Dam Kit, Model no. 60019066 - Product Usage: The dental dam forceps are intended to be used in conjunction with the rubber dental dam and the dental dam clamps. The forceps are used to place and remove the dental dam clamps from the rubber dental dam.

Multiple Coltene batches of the product have a pin size larger than acceptable, which may make it difficult for the forceps to fit appropriately with dental dam clamps.

ALL 50 STATES
▸Full report

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

Recall #:
85794
Lot/product code:
Batch numbers: J73571  If a distributor or end user received one of the batches listed above, they need to look at the batch number laser marked on the forceps themselves. If the forceps has any of the following batch numbers laser marked on them and the forceps do not fit with the dental dam clamps, the forceps should be returned to Coltene. Laser marked batch number:  1903 1904 1906 1907 1909 1910 1911 1915 1920 1921 1923 1927 1928 1930 1934 1940
Recalling firm:
Coltene Whaledent Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 3, 2020

HYGENIC Dental Dam Forceps, Model no. H01262 - Product Usage: The dental dam forceps are intended to be used in conjunction with the rubber dental dam and the dental dam clamps. The forceps are used to place and remove the dental dam clamps from the rubber dental dam.

Multiple Coltene batches of the product have a pin size larger than acceptable, which may make it difficult for the forceps to fit appropriately with dental dam clamps.

ALL 50 STATES
▸Full report

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

Recall #:
85794
Lot/product code:
Batch numbers: J16743 J16745 J29784 J31289 J33607 J44177 J44178 J44840 J47109 J47110 J49167 J67132 J73572 J73785 J74711  If a distributor or end user received one of the batches listed above, they need to look at the batch number laser marked on the forceps themselves. If the forceps has any of the following batch numbers laser marked on them and the forceps do not fit with the dental dam clamps, the forceps should be returned to Coltene. Laser marked batch number: 1903 1904 1906 1907 1909 1910 1911 1915 1920 1921 1923 1927 1928 1930 1934 1940
Recalling firm:
Coltene Whaledent Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 3, 2020

HYGENIC Wingless Fiesta Kit, Model no. H02790 - Product Usage: The dental dam forceps are intended to be used in conjunction with the rubber dental dam and the dental dam clamps. The forceps are used to place and remove the dental dam clamps from the rubber dental dam.

Multiple Coltene batches of the product have a pin size larger than acceptable, which may make it difficult for the forceps to fit appropriately with dental dam clamps.

ALL 50 STATES
▸Full report

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

Recall #:
85794
Lot/product code:
Batch numbers: J74546  J74184    If a distributor or end user received one of the batches listed above, they need to look at the batch number laser marked on the forceps themselves. If the forceps has any of the following batch numbers laser marked on them and the forceps do not fit with the dental dam clamps, the forceps should be returned to Coltene. Laser marked batch number:  1903 1904 1906 1907 1909 1910 1911 1915 1920 1921 1923 1927 1928 1930 1934 1940
Recalling firm:
Coltene Whaledent Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 4, 2020

Azure XT DR MRI, Model Numbers: a) W1DR01 and b) W2DR01

There is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i.e., battery measurements, Capture Management", Atrial Lead Position Check", EffectivCRT" algorithms, and AdaptivCRT"). This rare interaction results in temporary suspension of automatic threshold testing and output adjustments, and suspension of auto-optimization of CRT therapy. The issue is unlikely to result in clinical impact to the patient, and features are restored upon next programmer device interrogation or presence of a magnet.

ALL 50 STATES
▸Full report

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

Recall #:
85816
Lot/product code:
a) W1DR01, serial numbers: RNB200043H RNB200044H RNB200045H RNB200046H RNB200047H RNB200048H RNB200049H RNB200050H RNB200051H RNB200052H RNB200053H RNB200054H RNB200055H RNB200056H RNB200057H RNB200058H RNB200059H RNB200060H RNB200064H RNB200065H RNB200066H RNB200067H RNB200068H RNB200069H RNB200070H RNB200071H RNB200072H RNB200073H RNB200074H RNB200075H RNB200076H RNB200079H RNB200080H RNB200081H RNB200082H RNB200083H RNB200084H RNB200085H RNB200086H RNB200087H RNB200088H RNB200089H RNB200091H RNB200094H RNB200095H RNB200096H RNB200098H RNB200099H RNB200100H RNB200101H RNB200102H RNB200103H RNB200105H RNB200106H RNB200107H RNB200108H RNB200109H RNB200111H RNB200112H RNB200113H RNB200114H RNB200115H RNB200116H RNB200117H RNB200118H RNB200119H RNB200120H RNB200121H RNB200122H RNB200123H RNB200124H RNB200125H RNB200126H RNB200127H RNB200128H RNB200129H RNB200130H RNB200131H RNB200132H RNB200133H RNB200135H RNB200136H RNB200137H RNB200138H RNB200139H RNB200140H RNB200141H RNB200143H RNB200144H RNB200145H RNB200146H RNB200147H RNB200148H RNB200149H RNB200150H RNB200151H RNB200153H RNB200154H RNB200155H RNB200156H RNB200158H RNB200159H RNB200160H RNB200161H RNB200163H RNB200164H RNB200165H RNB200166H RNB200167H RNB200168H RNB200169H RNB200170H RNB200171H RNB200173H RNB200174H RNB200175H RNB200176H RNB200178H RNB200179H RNB200180H RNB200181H RNB200184H RNB200185H RNB200186H RNB200187H RNB200188H RNB200190H RNB200191H RNB200193H RNB200195H RNB200197H RNB200198H RNB200199H RNB200201H RNB200202H RNB200205H RNB200206H RNB200207H RNB200208H RNB200209H RNB200210H RNB200211H RNB200213H RNB200214H RNB200215H RNB200216H RNB200219H RNB200220H RNB200221H RNB200222H RNB200223H RNB200224H RNB200225H RNB200226H RNB200227H RNB200228H RNB200229H RNB200231H RNB200232H RNB200233H RNB200234H RNB200235H RNB200236H RNB200237H RNB200239H RNB200240H RNB200241H RNB200242H RNB200243H RNB200244H RNB200245H RNB200246H RNB200248H RNB200249H RNB200250H RNB200251H RNB200252H RNB200253H RNB200254H RNB200255H RNB200256H RNB200257H RNB200258H RNB200259H RNB200260H RNB200262H RNB200264H RNB200265H RNB200266H RNB200267H RNB200268H RNB200269H RNB200270H RNB200271H RNB200272H RNB200273H RNB200274H RNB200275H RNB200276H RNB200277H RNB200278H RNB200279H RNB200280H RNB200281H RNB200282H RNB200283H RNB200284H RNB200285H RNB200286H RNB200287H RNB200289H RNB200290H RNB200292H RNB200293H RNB200294H RNB200295H RNB200296H RNB200297H RNB200298H RNB200299H RNB200300H RNB200301H RNB200302H RNB200303H RNB200304H RNB200305H RNB200306H RNB200307H RNB200308H RNB200309H RNB200310H RNB200311H RNB200313H RNB200314H RNB200315H RNB200316H RNB200317H RNB200318H RNB200319H RNB200320H RNB200321H RNB200322H RNB200323H RNB200325H RNB200327H RNB200328H RNB200329H RNB200330H RNB200331H RNB200332H RNB200333H RNB200334H RNB200335H RNB200336H RNB200337H RNB200338H RNB200342H RNB200343H RNB200344H RNB200345H RNB200346H RNB200348H RNB200349H RNB200350H RNB200352H RNB200353H RNB200354H RNB200355H RNB200356H RNB200357H RNB200358H RNB200359H RNB200360H RNB200361H RNB200363H RNB200364H RNB200365H RNB200366H RNB200367H RNB200368H RNB200369H RNB200371H RNB200373H RNB200375H RNB200376H RNB200379H RNB200380H RNB200381H RNB200382H RNB200383H RNB200384H RNB200390H RNB200391H RNB200392H RNB200394H RNB200395H RNB200396H RNB200398H RNB200399H RNB200400H RNB200404H RNB200406H RNB200408H RNB200409H RNB200410H RNB200411H RNB200414H RNB200415H RNB200417H RNB200419H RNB200420H RNB200422H RNB200423H RNB200424H RNB200426H RNB200063H RNB200092H RNB200104H RNB200134H RNB200377H RNB200430H RNB200432H RNB200433H RNB200435H RNB200436H RNB200437H RNB200438H RNB200439H RNB200440H RNB200442H RNB200443H RNB200444H RNB200445H RNB200447H RNB200448H RNB200451H RNB200452H RNB200454H RNB200458H RNB200459H RNB200462H RNB200464H RNB200465H RNB200470H RNB200476H RNB200477H RNB200478H RNB200483H RNB200486H RNB200372H RNB200427H RNB200428H RNB200431H RNB200434H RNB200446H RNB200453H RNB200455H RNB200456H RNB200460H RNB200463H RNB200466H RNB200467H RNB200468H RNB200471H RNB200474H RNB200475H RNB200491H RNB200374H RNB200461H RNB200487H RNB200378H RNB200403H RNB200405H RNB200407H RNB200412H RNB200416H RNB200418H RNB200421H RNB200449H RNB200457H RNB200479H RNB200481H RNB200485H RNB200499H RNB200501H RNB200504H RNB200516H RNB200519H RNB200522H RNB200528H RNB200532H RNB200535H RNB200538H RNB200539H RNB200387H RNB200393H RNB200401H RNB200450H RNB200469H RNB200482H RNB200488H RNB200489H RNB200498H RNB200508H RNB200509H RNB200511H RNB200518H RNB200520H RNB200521H RNB200523H RNB200534H RNB200536H RNB200492H RNB200510H RNB200514H RNB200515H RNB200524H RNB200529H RNB200530H RNB200540H RNB200546H RNB200548H RNB200490H RNB200494H RNB200495H RNB200500H RNB200502H RNB200503H RNB200505H RNB200506H RNB200507H RNB200525H RNB200526H RNB200531H RNB200533H RNB200541H RNB200542H RNB200545H RNB200547H RNB200549H RNB200551H RNB200339H RNB200564H RNB200571H RNB200579H RNB200583H RNB200586H RNB200590H RNB200591H RNB200594H RNB200596H RNB200597H … (truncated, 2928830 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 4, 2020

Solara CRT-P MRI, Model Numbers: a) W1TR03, b) W1TR06, c) W4TR03, d) W4TR06

There is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i.e., battery measurements, Capture Management", Atrial Lead Position Check", EffectivCRT" algorithms, and AdaptivCRT"). This rare interaction results in temporary suspension of automatic threshold testing and output adjustments, and suspension of auto-optimization of CRT therapy. The issue is unlikely to result in clinical impact to the patient, and features are restored upon next programmer device interrogation or presence of a magnet.

ALL 50 STATES
▸Full report

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

Recall #:
85816
Lot/product code:
a) W1TR03, serial numbers: RNS200027H RNS200037H RNS200043H RNS200044H RNS200045H RNS200052H RNS200059H RNS200063H RNS200068H RNS200076H RNS200077H RNS200079H RNS200081H RNS200088H RNS200089H RNS200090H RNS200094H RNS200098H RNS200100H RNS200005H RNS200007H RNS200016H RNS200020H RNS200022H RNS200025H RNS200026H RNS200028H RNS200030H RNS200032H RNS200033H RNS200034H RNS200038H RNS200042H RNS200050H RNS200051H RNS200054H RNS200060H RNS200061H RNS200064H RNS200065H RNS200067H RNS200071H RNS200072H RNS200074H RNS200080H RNS200082H RNS200084H RNS200085H RNS200086H RNS200087H RNS200091H RNS200093H RNS200099H RNS200101H RNS200053H RNS200104H RNS200109H RNS200111H RNS200116H RNS200118H RNS200019H RNS200040H RNS200092H RNS200035H RNS200102H RNS200103H RNS200105H RNS200107H RNS200108H RNS200110H RNS200113H RNS200115H RNS200117H RNS200119H RNS200120H RNS200121H RNS200122H RNS200123H RNS200125H RNS200126H RNS200127H RNS200048H RNS200128H RNS200130H RNS200140H RNS200124H RNS200129H RNS200143H RNS200144H RNS200131H RNS200138H RNS200132H RNS200136H RNS200137H RNS200133H RNS200134H RNS200135H RNS200148H RNS200149H RNS200150H RNS200151H RNS200154H RNS200155H RNS200156H RNS200158H RNS200159H RNS200160H RNS200161H RNS200162H RNS200163H RNS200164H RNS200165H RNS200167H RNS200168H RNS200169H RNS200170H RNS200171H RNS200172H RNS200173H RNS200174H RNS200175H RNS200176H RNS200177H RNS200178H RNS200179H RNS200181H RNS200185H RNS200193H RNS200194H RNS200195H RNS200196H RNS200198H RNS200199H RNS200202H RNS200203H RNS200204H RNS200206H RNS200207H RNS200210H RNS200212H RNS200213H RNS200214H RNS200215H RNS200216H RNS200217H RNS200220H RNS200223H RNS200224H RNS200226H RNS200227H RNS200228H RNS200230H RNS200232H RNS200182H RNS200183H RNS200186H RNS200191H RNS200200H RNS200205H RNS200229H RNS200231H RNS200142H RNS200218H RNS200233H RNS200234H RNS200235H RNS200236H RNS200237H RNS200239H RNS200240H RNS200243H RNS200245H RNS200246H RNS200247H RNS200248H RNS200251H RNS200252H RNS200253H RNS200255H RNS200256H RNS200258H RNS200259H RNS200260H RNS200242H RNS200238H RNS200296H RNS200299H RNS200301H RNS200302H RNS200307H RNS200335H RNS200340H RNS200350H RNS200359H RNS200369H RNS200187H RNS200309H RNS200311H RNS200313H RNS200314H RNS200316H RNS200318H RNS200321H RNS200327H RNS200329H RNS200330H RNS200331H RNS200332H RNS200333H RNS200334H RNS200336H RNS200337H RNS200345H RNS200346H RNS200347H RNS200348H RNS200349H RNS200353H RNS200355H RNS200356H RNS200360H RNS200363H RNS200364H RNS200367H RNS200368H RNS200266H RNS200268H RNS200273H RNS200275H RNS200281H RNS200283H RNS200286H RNS200287H RNS200289H RNS200291H RNS200293H RNS200324H RNS200325H RNS200339H RNS200343H RNS200357H RNS200361H RNS200010H RNS200262H RNS200263H RNS200264H RNS200265H RNS200267H RNS200270H RNS200274H RNS200276H RNS200278H RNS200279H RNS200280H RNS200288H RNS200290H RNS200303H RNS200315H RNS200317H RNS200319H RNS200326H RNS200370H RNS200284H RNS200285H RNS200294H RNS200298H RNS200306H RNS200310H RNS200341H RNS200354H RNS200365H RNS200391H RNS200392H RNS200393H RNS200394H RNS200398H RNS200401H RNS200402H RNS200405H RNS200376H RNS200380H RNS200382H RNS200383H RNS200385H RNS200389H RNS200399H RNS200372H RNS200373H RNS200374H RNS200377H RNS200381H RNS200384H RNS200388H RNS200390H RNS200395H RNS200396H RNS200397H RNS200400H RNS200297H RNS200145H RNS200407H RNS200408H RNS200410H RNS200412H RNS200413H RNS200414H RNS200420H RNS200421H RNS200422H RNS200423H RNS200424H RNS200430H RNS200406H RNS200409H RNS200411H RNS200415H RNS200418H RNS200425H RNS200426H RNS200427H RNS200428H RNS200432H RNS200440H RNS200449H RNS200451H RNS200454H RNS200434H RNS200435H RNS200444H RNS200446H RNS200448H RNS200450H RNS200455H RNS200456H RNS200433H RNS200436H RNS200437H RNS200438H RNS200439H RNS200441H RNS200442H RNS200443H RNS200445H RNS200453H RNS200338H RNS200459H RNS200461H RNS200462H RNS200463H RNS200464H RNS200465H RNS200466H RNS200467H RNS200468H RNS200469H RNS200471H RNS200472H RNS200473H RNS200474H RNS200475H RNS200476H RNS200477H RNS200479H RNS200480H RNS200481H RNS200482H RNS200484H RNS200485H RNS200486H RNS200487H RNS200488H RNS200489H RNS200490H RNS200491H RNS200492H RNS200494H RNS200495H RNS200457H RNS200493H RNS200496H RNS200497H RNS200498H RNS200501H RNS200505H RNS200506H RNS200507H RNS200503H RNS200504H RNS200510H RNS200508H RNS200509H RNS200511H RNS200512H RNS200521H RNS200525H RNS200528H RNS200532H RNS200564H RNS200571H RNS200523H RNS200526H RNS200527H RNS200563H RNS200567H RNS200515H RNS200514H RNS200516H RNS200517H RNS200519H RNS200531H RNS200536H RNS200553H RNS200558H RNS200561H RNS200565H RNS200566H RNS200529H RNS200533H RNS200534H RNS200537H RNS200541H RNS200546H RNS200548H RNS200551H RNS200555H RNS200568H RNS200569H RNS200572H RNS200556H RNS200573H RNS200578H RNS200581H RNS200588H RNS200591H RNS200597H RNS200600H RNS200610H RNS200615H RNS200618H RNS200621H RNS200623H RNS200624H RNS200628H RNS200629H RNS200547H RNS200574H RNS200576H RNS200579H RNS200582H RNS200583H RNS200585H RNS200587H R… (truncated, 183447 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 4, 2020

Serena CRT-P MRI, Model Numbers: a) W1TR02, b) W1TR05, c) W4TR02, d) W4TR05

There is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i.e., battery measurements, Capture Management", Atrial Lead Position Check", EffectivCRT" algorithms, and AdaptivCRT"). This rare interaction results in temporary suspension of automatic threshold testing and output adjustments, and suspension of auto-optimization of CRT therapy. The issue is unlikely to result in clinical impact to the patient, and features are restored upon next programmer device interrogation or presence of a magnet.

ALL 50 STATES
▸Full report

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

Recall #:
85816
Lot/product code:
a) W1TR02, serial numbers: RNQ200008H RNQ200032H RNQ200035H RNQ200043H RNQ200045H RNQ200049H RNQ200051H RNQ200052H RNQ200057H RNQ200059H RNQ200061H RNQ200074H RNQ200076H RNQ200080H RNQ200096H RNQ200100H RNQ200102H RNQ200107H RNQ200109H RNQ200110H RNQ200111H RNQ200130H RNQ200132H RNQ200133H RNQ200003H RNQ200005H RNQ200006H RNQ200007H RNQ200010H RNQ200011H RNQ200017H RNQ200018H RNQ200020H RNQ200022H RNQ200025H RNQ200028H RNQ200029H RNQ200031H RNQ200033H RNQ200034H RNQ200036H RNQ200039H RNQ200040H RNQ200050H RNQ200054H RNQ200056H RNQ200060H RNQ200062H RNQ200064H RNQ200065H RNQ200067H RNQ200071H RNQ200072H RNQ200075H RNQ200077H RNQ200078H RNQ200081H RNQ200085H RNQ200088H RNQ200091H RNQ200093H RNQ200098H RNQ200103H RNQ200105H RNQ200108H RNQ200115H RNQ200116H RNQ200119H RNQ200120H RNQ200123H RNQ200124H RNQ200125H RNQ200126H RNQ200128H RNQ200131H RNQ200135H RNQ200137H RNQ200141H RNQ200145H RNQ200146H RNQ200147H RNQ200152H RNQ200154H RNQ200157H RNQ200158H RNQ200162H RNQ200167H RNQ200168H RNQ200169H RNQ200171H RNQ200174H RNQ200012H RNQ200134H RNQ200136H RNQ200139H RNQ200140H RNQ200183H RNQ200149H RNQ200150H RNQ200159H RNQ200160H RNQ200163H RNQ200176H RNQ200178H RNQ200179H RNQ200180H RNQ200181H RNQ200186H RNQ200188H RNQ200189H RNQ200198H RNQ200199H RNQ200206H RNQ200210H RNQ200217H RNQ200229H RNQ200234H RNQ200238H RNQ200245H RNQ200247H RNQ200248H RNQ200249H RNQ200196H RNQ200202H RNQ200204H RNQ200212H RNQ200221H RNQ200230H RNQ200235H RNQ200244H RNQ200191H RNQ200200H RNQ200203H RNQ200233H RNQ200192H RNQ200193H RNQ200194H RNQ200195H RNQ200208H RNQ200215H RNQ200231H RNQ200241H RNQ200302H RNQ200246H RNQ200274H RNQ200275H RNQ200280H RNQ200281H RNQ200282H RNQ200283H RNQ200284H RNQ200285H RNQ200286H RNQ200287H RNQ200303H RNQ200307H RNQ200272H RNQ200278H RNQ200292H RNQ200251H RNQ200255H RNQ200259H RNQ200261H RNQ200262H RNQ200265H RNQ200266H RNQ200300H RNQ200250H RNQ200256H RNQ200258H RNQ200263H RNQ200267H RNQ200277H RNQ200254H RNQ200260H RNQ200264H RNQ200269H RNQ200291H RNQ200374H RNQ200387H RNQ200368H RNQ200369H RNQ200376H RNQ200383H RNQ200384H RNQ200385H RNQ200386H RNQ200373H RNQ200227H RNQ200370H RNQ200372H RNQ200375H RNQ200378H RNQ200379H RNQ200389H RNQ200394H RNQ200381H RNQ200398H RNQ200399H RNQ200404H RNQ200405H RNQ200400H RNQ200401H RNQ200402H RNQ200403H RNQ200430H RNQ200432H RNQ200433H RNQ200434H RNQ200436H RNQ200438H RNQ200444H RNQ200449H RNQ200450H RNQ200408H RNQ200409H RNQ200443H RNQ200456H RNQ200417H RNQ200420H RNQ200427H RNQ200407H RNQ200410H RNQ200413H RNQ200414H RNQ200415H RNQ200421H RNQ200423H RNQ200426H RNQ200459H RNQ200462H RNQ200425H RNQ200460H RNQ200411H RNQ200471H RNQ200475H RNQ200416H RNQ200418H RNQ200429H RNQ200457H RNQ200463H RNQ200464H RNQ200472H RNQ200474H RNQ200519H RNQ200442H RNQ200446H RNQ200467H RNQ200468H RNQ200490H RNQ200494H RNQ200499H RNQ200465H RNQ200479H RNQ200480H RNQ200482H RNQ200485H RNQ200487H RNQ200495H RNQ200497H RNQ200502H RNQ200507H RNQ200509H RNQ200512H RNQ200514H RNQ200516H RNQ200520H RNQ200524H RNQ200470H RNQ200473H RNQ200477H RNQ200484H RNQ200491H RNQ200492H RNQ200496H RNQ200501H RNQ200466H RNQ200481H RNQ200486H RNQ200488H RNQ200489H RNQ200508H RNQ200513H RNQ200515H RNQ200454H RNQ200510H RNQ200518H RNQ200435H RNQ200448H RNQ200469H RNQ200493H RNQ200526H RNQ200527H RNQ200529H RNQ200530H RNQ200533H RNQ200534H RNQ200535H RNQ200541H RNQ200544H RNQ200547H RNQ200553H RNQ200554H RNQ200531H RNQ200542H RNQ200558H RNQ200561H RNQ200546H RNQ200549H RNQ200555H RNQ200537H RNQ200540H RNQ200545H RNQ200565H RNQ200570H RNQ200589H RNQ200252H RNQ200569H RNQ200601H RNQ200568H RNQ200597H RNQ200595H RNQ200605H RNQ200603H RNQ200604H RNQ200607H RNQ200609H RNQ200610H RNQ200633H RNQ200634H RNQ200636H RNQ200638H RNQ200643H RNQ200644H RNQ200645H RNQ200646H RNQ200648H RNQ200635H RNQ200640H RNQ200614H RNQ200618H RNQ200623H RNQ200625H RNQ200626H RNQ200632H RNQ200637H RNQ200650H RNQ200651H RNQ200652H RNQ200613H RNQ200615H RNQ200616H RNQ200617H RNQ200619H RNQ200620H RNQ200621H RNQ200622H RNQ200624H RNQ200627H RNQ200628H RNQ200629H RNQ200630H RNQ200631H RNQ200653H RNQ200660H RNQ200667H RNQ200669H RNQ200654H RNQ200658H RNQ200661H RNQ200668H RNQ200671H RNQ200190H RNQ200655H RNQ200659H RNQ200662H RNQ200664H RNQ200665H RNQ200670H RNQ200656H RNQ200673H RNQ200674H RNQ200675H RNQ200676H RNQ200677H RNQ200679H RNQ200680H RNQ200681H RNQ200682H RNQ200688H RNQ200689H RNQ200692H RNQ200701H RNQ200702H RNQ200704H RNQ200707H RNQ200683H RNQ200687H RNQ200690H RNQ200693H RNQ200694H RNQ200695H RNQ200697H RNQ200698H RNQ200699H RNQ200700H RNQ200703H RNQ200709H RNQ200710H RNQ200711H RNQ200712H RNQ200714H RNQ200715H RNQ200716H RNQ200717H RNQ200718H RNQ200721H RNQ200722H RNQ200723H RNQ200724H RNQ200727H RNQ200728H RNQ200729H RNQ200731H RNQ200732H RNQ200733H RNQ200734H RNQ200735H RNQ200737H RNQ200738H RNQ200740H RNQ200741H RNQ200742H RNQ200743H RNQ200744H RNQ200747H RNQ200749H RNQ200750H RNQ200752H RNQ200753H RNQ200756H RNQ200759H RNQ200760H RNQ200761H RNQ200762H RNQ200763H RNQ200765H RNQ200766H RNQ200767H RNQ200686H RNQ200708H RNQ200770H R… (truncated, 195361 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 4, 2020

Azure S SR MRI, Model Number W3SR01

There is a rare communication sequence during the first device interrogation with a SmartSync Device Manager that may result in the temporary suspension of some device features (i.e., battery measurements, Capture Management", Atrial Lead Position Check", EffectivCRT" algorithms, and AdaptivCRT"). This rare interaction results in temporary suspension of automatic threshold testing and output adjustments, and suspension of auto-optimization of CRT therapy. The issue is unlikely to result in clinical impact to the patient, and features are restored upon next programmer device interrogation or presence of a magnet.

ALL 50 STATES
▸Full report

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

Recall #:
85816
Lot/product code:
serial numbers: RNI200028H RNI200029H RNI200031H RNI200033H RNI200034H RNI200037H RNI200038H RNI200039H RNI200041H RNI200042H RNI200043H RNI200044H RNI200045H RNI200046H RNI200048H RNI200050H RNI200051H RNI200053H RNI200054H RNI200055H RNI200057H RNI200058H RNI200059H RNI200061H RNI200063H RNI200064H RNI200065H RNI200066H RNI200067H RNI200069H RNI200071H RNI200072H RNI200076H RNI200077H RNI200078H RNI200079H RNI200080H RNI200081H RNI200082H RNI200083H RNI200084H RNI200085H RNI200086H RNI200087H RNI200088H RNI200089H RNI200090H RNI200091H RNI200094H RNI200095H RNI200096H RNI200097H RNI200098H RNI200099H RNI200100H RNI200101H RNI200102H RNI200103H RNI200104H RNI200105H RNI200106H RNI200107H RNI200108H RNI200109H RNI200111H RNI200112H RNI200113H RNI200115H RNI200118H RNI200119H RNI200121H RNI200122H RNI200123H RNI200124H RNI200125H RNI200126H RNI200127H RNI200128H RNI200130H RNI200132H RNI200134H RNI200135H RNI200137H RNI200138H RNI200139H RNI200140H RNI200141H RNI200142H RNI200144H RNI200146H RNI200147H RNI200148H RNI200149H RNI200150H RNI200151H RNI200152H RNI200155H RNI200156H RNI200157H RNI200158H RNI200159H RNI200160H RNI200161H RNI200162H RNI200163H RNI200164H RNI200166H RNI200167H RNI200168H RNI200169H RNI200170H RNI200171H RNI200172H RNI200173H RNI200174H RNI200175H RNI200180H RNI200181H RNI200182H RNI200183H RNI200184H RNI200186H RNI200187H RNI200188H RNI200195H RNI200202H RNI200203H RNI200116H RNI200143H RNI200177H RNI200178H RNI200191H RNI200192H RNI200193H RNI200194H RNI200196H RNI200197H RNI200198H RNI200199H RNI200200H RNI200201H RNI200060H RNI200092H RNI200210H RNI200211H RNI200214H RNI200236H RNI200241H RNI200243H RNI200270H RNI200273H RNI200280H RNI200282H RNI200300H RNI200302H RNI200303H RNI200304H RNI200305H RNI200312H RNI200313H RNI200315H RNI200327H RNI200330H RNI200335H RNI200347H RNI200359H RNI200371H RNI200208H RNI200209H RNI200219H RNI200230H RNI200232H RNI200240H RNI200268H RNI200284H RNI200287H RNI200296H RNI200326H RNI200338H RNI200363H RNI200372H RNI200255H RNI200265H RNI200278H RNI200344H RNI200348H RNI200349H RNI200350H RNI200351H RNI200353H RNI200354H RNI200356H RNI200357H RNI200360H RNI200388H RNI200408H RNI200310H RNI200325H RNI200380H RNI200245H RNI200246H RNI200248H RNI200249H RNI200250H RNI200251H RNI200254H RNI200256H RNI200257H RNI200258H RNI200260H RNI200261H RNI200263H RNI200264H RNI200266H RNI200271H RNI200274H RNI200275H RNI200277H RNI200279H RNI200381H RNI200382H RNI200383H RNI200384H RNI200385H RNI200387H RNI200389H RNI200390H RNI200392H RNI200394H RNI200395H RNI200396H RNI200397H RNI200398H RNI200399H RNI200401H RNI200402H RNI200403H RNI200404H RNI200405H RNI200407H RNI200411H RNI200412H RNI200414H RNI200416H RNI200417H RNI200418H RNI200420H RNI200421H RNI200423H RNI200424H RNI200425H RNI200427H RNI200429H RNI200430H RNI200432H RNI200435H RNI200436H RNI200437H RNI200438H RNI200439H RNI200440H RNI200221H RNI200319H RNI200362H RNI200204H RNI200205H RNI200206H RNI200207H RNI200212H RNI200213H RNI200216H RNI200217H RNI200218H RNI200220H RNI200222H RNI200223H RNI200224H RNI200226H RNI200227H RNI200228H RNI200229H RNI200231H RNI200234H RNI200235H RNI200237H RNI200238H RNI200242H RNI200269H RNI200281H RNI200285H RNI200290H RNI200297H RNI200298H RNI200299H RNI200301H RNI200308H RNI200309H RNI200311H RNI200317H RNI200328H RNI200329H RNI200336H RNI200340H RNI200341H RNI200345H RNI200352H RNI200355H RNI200358H RNI200364H RNI200366H RNI200368H RNI200370H RNI200373H RNI200374H RNI200375H RNI200376H RNI200378H RNI200379H RNI200393H RNI200410H RNI200215H RNI200276H RNI200337H RNI200365H RNI200441H RNI200442H RNI200444H RNI200445H RNI200446H RNI200448H RNI200449H RNI200459H RNI200460H RNI200461H RNI200462H RNI200463H RNI200465H RNI200466H RNI200467H RNI200468H RNI200447H RNI200450H RNI200451H RNI200453H RNI200454H RNI200455H RNI200456H RNI200464H RNI200470H RNI200472H RNI200474H RNI200475H RNI200476H RNI200477H RNI200478H RNI200479H RNI200482H RNI200484H RNI200486H RNI200487H RNI200488H RNI200489H RNI200490H RNI200491H RNI200492H RNI200493H RNI200494H RNI200496H RNI200498H RNI200499H RNI200501H RNI200502H RNI200503H RNI200504H RNI200505H RNI200506H RNI200507H RNI200508H RNI200509H RNI200510H RNI200511H RNI200512H RNI200513H RNI200514H RNI200515H RNI200070H RNI200036H RNI200133H RNI200176H RNI200286H RNI200516H RNI200518H RNI200519H RNI200520H RNI200521H RNI200523H RNI200524H RNI200525H RNI200526H RNI200528H RNI200529H RNI200530H RNI200532H RNI200533H RNI200535H RNI200537H RNI200538H RNI200539H RNI200542H RNI200543H RNI200544H RNI200545H RNI200546H RNI200547H RNI200548H RNI200549H RNI200553H RNI200554H RNI200555H RNI200556H RNI200557H RNI200558H RNI200559H RNI200560H RNI200561H RNI200565H RNI200566H RNI200567H RNI200568H RNI200569H RNI200570H RNI200572H RNI200573H RNI200574H RNI200575H RNI200579H RNI200580H RNI200582H RNI200583H RNI200584H RNI200585H RNI200586H RNI200587H RNI200590H RNI200591H RNI200593H RNI200594H RNI200595H RNI200596H RNI200597H RNI200599H RNI200602H RNI200604H … (truncated, 131499 characters total — see the official FDA record for the full value)
Recalling firm:
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
View official FDA record (opens in a new tab)