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Recalls affecting Nebraska

Data last updated: September 10, 2026 at 1:16 PM UTC

16,502 recalls found

Just announced

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

Business Pill, Branch Manager for Mendietary 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 AliveMoringa 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. Braun0.9% 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 ValueOrganic 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)
UnclassifiedAllergenMilkUndeclaredAnnounced August 31, 2026

Little TemptationsChocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

Full report
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

LipofitLipofit 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

KofinasGarlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

Full report
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 SproutsRobust 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

MartinaMangoes

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 January 15, 2021

CervAlign Anterior Cervical Plate System-Cervalign, 2Level, 24mm Material Number: 66-224 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies, spondylolisthesis, trauma (i.e. fracture or dislocation), spinal stenosis, deformities or curvatures (i.e. scoliosis, kyphosis, and/or lordosis), tumor, pseudathrosis, and failed previous fusion).

Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

ALL 50 STATES
Full report

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

Recall #:
87251
Lot/product code:
Batch Number: 330510 330511 338826 344094 350507 355018 361793 361794 364054 372180 372181 377184 378427
Recalling firm:
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 15, 2021

CervAlign Anterior Cervical Plate System-Cervalign, 5 Level, 105mm Material Number: 66-5105 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies, spondylolisthesis, trauma (i.e. fracture or dislocation), spinal stenosis, deformities or curvatures (i.e. scoliosis, kyphosis, and/or lordosis), tumor, pseudathrosis, and failed previous fusion).

Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

ALL 50 STATES
Full report

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

Recall #:
87251
Lot/product code:
Batch Number: 345228 352383 357124 364542 370440 382120
Recalling firm:
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 15, 2021

CervAlign Anterior Cervical Plate System-Cervalign, 4Level, 64mm Material Number: 66-464 - Product Usage: intended for anterior cervical fixation (C2-C7) for the following conditions: degenerative disc disease (DDD) defined as neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies, spondylolisthesis, trauma (i.e. fracture or dislocation), spinal stenosis, deformities or curvatures (i.e. scoliosis, kyphosis, and/or lordosis), tumor, pseudathrosis, and failed previous fusion).

Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

ALL 50 STATES
Full report

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

Recall #:
87251
Lot/product code:
Batch Number: 342453 348028 351951 357126 364538 370411 380157
Recalling firm:
RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 19, 2021

Stryker Sustainability Solutions REF HARH36 Ethicon Endo-Surgery, Inc. Harmonic ACE +7, Shears with Advanced Hemostasis 5mm Diameter x 36cm - Product Usage: indicated for soft tissue incisions when bleeding control and minimal thermal injury are desired. The instruments can be used as an adjunct to or substitute for electrosurgery, lasers and steel scalpels in general, plastic, pediatric, gynecologic, urologic, thoracic, exposure to orthopedic structures (such as spine and joint space), sealing and transection of lymphatic vessels, and other open and endoscopic procedures.

Product was distributed without receiving regulatory clearance.

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Full report

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

Recall #:
87434
Lot/product code:
Catalog Number: HARH36 GTIN: 07613327346251 Lot Number: 12444050
Recalling firm:
Stryker Sustainability Solutions
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 19, 2021

Captivator Single-Use Polypectomy Snares, Captiflex Single-Use Polypectomy Snares. Outer box UPN, Inner Pouch UPN: M00561311 (Box 10), M00561310 M00562301 (Box 10), M00562300; M00562321 (Box 10), M00562320; M00562341 (Box 10), M00562340; M00562451 (Box 10), M00562450; M00562401 (Box 10), M00562400; M00562402 (Box 40), M00562400; M00562422 (Box 40), M00562420; M00562471 (Box 10), M00562470.

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

ALL 50 STATES
Full report

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

Recall #:
87221
Lot/product code:
Outer box GTIN: 08714729019251 Inner pouch GTIN: 08714729747680 Lot/Batch#: 24725319, 24782695,   Outer box GTIN: 08714729019312 Inner pouch GTIN: 08714729747833 Lot/Batch#: 24842597, 24812577,   Outer box GTIN: 08714729019336 Inner pouch GTIN: 08714729747857 Lot/Batch#: 24889757, 24719202, 24709536, 24773287,   Outer box GTIN: 08714729019350 Inner pouch GTIN: 08714729747871 Lot/Batch#: 24782693, 24732964, 24889755, 24780939,   Outer box GTIN: 08714729071068 Inner pouch GTIN: 08714729747970 Lot/Batch#: 24882357, 24782689, 24782687, 24729758,   Outer box GTIN: 08714729019411 Inner pouch GTIN:08714729747932 Lot/Batch#: 24961643  Outer box GTIN:08714729501640 Inner pouch GTIN: 08714729747932 Lot/Batch#: 24961645, 24989260, 24844193,   Outer box GTIN:08714729501657 Inner pouch GTIN:08714729747956 Lot/Batch#: 25010054,   Outer box GTIN:08714729019459 Inner pouch GTIN:08714729747994 Lot/Batch#: 25016793.
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 19, 2021

Various reprocessed products: PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO; PROVISION Reprocessed Depy Mitek Ablation Electrodes, VAPR COOLPULSE 90 deg; PROVISION Reprocessed Smith and Nephew Trocars/ Cannulas (Class I); PROVISION Reprocessed Conmed/ Linvatec Suture Retrievers/ Passers C6387 See updated product list attached for details.

Non-sterile product was shipped to customers labelled as sterile.

ALL 50 STATES
Full report

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

Recall #:
87258
Lot/product code:
Lot Number L-008926-16037 Lot numbers L-008918-16048, and L-008918-16045  Lot numbers L-008936-16275, and L-008933-16078
Recalling firm:
ReNovo, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 19, 2021

Enteral Infusion Pump

The potential for air appearing in the enteral feed pumping set tubing during set-up.

ALL 50 STATES
Full report

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

Recall #:
87281
Lot/product code:
Catalog Number: 612054, 613650, 614650, 672055, 673656, 673662, 674655, 674668, 674669, 716154, 762055, 763656, 763662, 765100, 765559, 772055, 773656, 773662, 775100, 775659, 776150
Recalling firm:
Cardinal Health 200, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 19, 2021

Captivator II Single-Use Polypectomy Snares Outer box UPN, Inner Pouch UPN: M00561191 (Box 10), M00561190; M00561221 (Box 10), M00561220; M00561222 (Box 20), M00561220; M00561223 (Box 40), M00561220; M00561233 (Box 40), M00561230.

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

ALL 50 STATES
Full report

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

Recall #:
87221
Lot/product code:
Outer box GTIN: 08714729855934 Inner pouch GTIN: 08714729861263 Lot/Batch#: 25053639  Outer box GTIN: 08714729855903 Inner pouch GTIN: 08714729861294 Lot/Batch#: 24948407, 24670592, 24679619, 24676929, 24939628  Outer box GTIN: 08714729861300 Inner pouch GTIN: 087147298 61294 Lot/Batch#: 24770325, 24952552, 24665104  Outer box GTIN: 08714729861317 Inner pouch GTIN: 08714729861294 Lot/Batch#: 24679614, 25054403  Outer box GTIN: 08714729861348 Inner pouch GTIN: 08714729861324 Lot/Batch#: 24772995
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 19, 2021

Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670; M00562672 (Box 20), M00562670; M00562673 (Box 40), M00562670; M00562691 (Box 5); M00562690; M00562692 (Box 20), M00562690; M00562693 (Box 40), M00562690.

Packaging Incomplete Seal. Users noted an incomplete pouch seal prior to using the device in a patient.

ALL 50 STATES
Full report

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

Recall #:
87221
Lot/product code:
Outer box GTIN: 08714729283904 Inner pouch GTIN: 08714729747598 Lot/Batch#: 24818278, 24906823, 25042455  Outer box GTIN: 08714729283928 Inner pouch GTIN: 08714729747611 Lot/Batch#: 24685766, 24817145, 24899710, 24739786, 25006735, 24861901  Outer box GTIN: 08714729158110 Inner pouch GTIN: 08714729748069 Lot/Batch#: 24685764, 24890051, 24824132  Outer box GTIN: 08714729268802 Inner pouch GTIN: 08714729748069 Lot/Batch#: 25023345  Outer box GTIN: 08714729158141 Inner pouch GTIN: 08714729748083 Lot/Batch#: 24699718, 24939626, 24861739  Outer box GTIN: 08714729268819 Inner pouch GTIN: 08714729748083 Lot/Batch#: 24824134, 25006729, 24709534  Outer box GTIN: 08714729501664 Inner pouch GTIN: 08714729748083 Lot/Batch#: 25023203, 24697822, 24739587, 24942292, 24909214, 24824136  Outer box GTIN: 08714729158158 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24856636, 24927642, 24699218  Outer box GTIN: 08714729268826 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24835709, 24818605, 25023343  Outer box GTIN: 08714729501671 Inner pouch GTIN: 08714729748106 Lot/Batch#: 24909216, 24758832, 24872119, 24994171, 25048397, 2475126, 24929431, 24995438
Recalling firm:
Boston Scientific Corporation
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled January 25, 2021

Metformin Hydrochloride Extended-Release Tablets, USP, 750 mg, 100 Tablets per bottle, Rx Only, Manufactured by: Nostrum Laboratories, Inc., Kansas City, MO 64120. NDC: 29033-056-01

CGMP Deviations: detection of 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-0249-2021
Lot/product code:
Lot MET200601, 07/2022
Recalling firm:
Nostrum Laboratories Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled January 27, 2021

Spironolactone Tablets, USP, 25 mg, packaged in: a) 30-count bottles (NDC 63629-1064-01), b) 60-count bottles (NDC 63629-1064-02), c) 90-count bottles (NDC 63629-1064-03), Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0303-2021
Lot/product code:
a) Lot #: 148969, Exp 7/31/2022, b) Lot #: 148791, Exp 7/31/2022, c) Lot #: 148991, Exp 7/31/2022
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled January 27, 2021

Spironolactone Tablets, USP, 50 mg, packaged in 30-count bottles, Rx only, Manufactured by: Frontida BioPharm, Inc., Philadelphia, PA 19124 USA, Repackaged by: Bryant Ranch Prepack, Inc., Burbank, CA 91504 USA, NDC 63629-1067-01

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 50 mg may contain spironolactone 25 mg tablets.

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-0304-2021
Lot/product code:
Lot #: 148992, Exp 5/31/2022
Recalling firm:
Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled January 29, 2021

S-Series Equipment Management System; Model Number(s):0682400550; UDI: 07613327400502 Components that are affected within the S-Series Finished Good Model Number o P38198 - ASM, MFR CONTROLLER, FIXED STANDARD o P38199 - ASM, MFR CONTROLLER, LIFT STANDARD o P40553 - ASM, MFR HANDLE REPAIR, LIFTING, S-SERIES, STANDARD o P40554 - ASM, MFR HANDLE REPAIR, FIXED, S-SERIES, STANDARD o P46269 - ASSY, MFR CONTROLLER UPGRADE, STANDARD

The manufacturer has become aware that there is a likelihood that the S-Series Equipment Management System Capacitive Touch Controls on the MFRs rotational electrical magnetic brakes may disengage when an electrocautery device is in use.

ALL 50 STATES
Full report

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

Recall #:
87331
Lot/product code:
Serial Numbers: 2258046 2863490
Recalling firm:
Stryker Communications
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 1, 2021

Velocity Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.

ALL 50 STATES
Full report

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

Recall #:
87274
Lot/product code:
Catalog Numbers 7201 (lots 0217H, 0317J, 0417B, 0417F, 0417H, 0618K, 0718B, 0718D, 0718F, 0419J, 0519J, 0120F, 0420B, 0720K, 0720M, 0820L, 0117D, 0117F, 1020L); 7205 (lots 0217B, 0317L); 7206 (lots 0217B, 0317L); 7201-01 (lots 0920B, 0920D, 0920H); 7203 (0217F, 0317B, 0317L, 0417H).
Recalling firm:
Bovie Medical Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 1, 2021

HNM Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.

ALL 50 STATES
Full report

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

Recall #:
87274
Lot/product code:
Catalog Numbers HNM-31-150365 (lots 1017G, 1117B, 1217B, 0418C, 0518D, 0518H, 0618B, 0618D, 0818E, 1018J, 1018M, 1118J, 1218B, 1119B, 0420H, 0820H); HNM-31-150367 (lot 1117D); HNM-31-150368 (lot 1117D).
Recalling firm:
Bovie Medical Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 1, 2021

ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.

There can be a potential breach of the sterile packaging barrier due to the development of pinholes at the crease of the double-folded edge of the current package configuration.

ALL 50 STATES
Full report

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

Recall #:
87274
Lot/product code:
Catalog Numbers C3390A (lots 0317F, 0417B, 0517B, 0517D, 0517J, 0617D, 0617F, 0617H, 0617K, 0717A, 0717G, 0817B, 0917G, 0917J, 1017C, 1017E, 1017J, 1117B, 0418C); C3350A (lots 0317F, 0417B, 0517B, 0517G, 0717C, 0817D, 0917C, 0917E); C3350NA (lots 0317F, 0517G, 0817F); C2455NA (lots 0317F, 0517B, 0717E, 1017C, 1017E); C1860NA (lots 0317F, 0517B, 0717E, 0817F, 1017G, 0418E); C3390NA (lots 0317F, 0517G, 0817H, 1017J, 0418E, 0518F, 1218C).
Recalling firm:
Bovie Medical Corporation
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 2, 2021

Enoxaparin Sodium Injection, USP 120 mg/ 0.8 mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 0.8 mL Single Dose Syringes Rx Only,Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-0796-4 UPC 360505079543 (carton) NDC 60505-0796-0 UPC (01)10360505079602 (label)

Labeling; Label Mixup; syringe barrels may contain markings for 100 mg/mL (corresponding to 100 mg/mL strength) instead of 150 mg/mL (corresponding to 120 mg/0.8mL strength)

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0262-2021
Lot/product code:
Batch: CT003 Exp. 05/2022
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled February 2, 2021

Enoxaparin Sodium Injection, USP 100 mg/mL Single Dose Syringes with Automatic Safety Device For Subcutaneous Injection 10 x 1 mL Single Dose Syringes Rx Only, Manufactured by: Gland Pharma Ltd. Hyderabad, India Manufactured for: Apotex Corp. Weston, FL 33326 NDC 60505-0795-4 UPC 360505079544 (carton) NDC 60505-0795-1 UPC (01)10360505079510 (label)

Labeling; Label Mixup; syringe barrels may containing markings for 150 mg/mL (corresponding to 120 mg/0.8mL strength) instead of 100 mg/mL markings (corresponding to 100 mg/mL strength)

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0261-2021
Lot/product code:
Batch: CS008 Exp. 04/2022
Recalling firm:
Apotex Corp.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 3, 2021

Implantable cardioverter defibrillators (ICD) with cardiac resynchronization therapy (CRT-D): 1) Viva family: Viva XT CRT-D, Viva XT Quad CRT-D, Viva S CRT-D, Viva Quad S CRT-D and Viva Quad C CRT-D models; 2) Claria family: Claria MRI CRT-D and Claria MRI Quad CRT-D models; 3) Amplia family: Amplia MRI CRT-D and Amplia MRI Quad CRT-D models; 4) Compia family: Compia MRI CRT-D model; 5) Brava family: Brava CRT-D and Brava Quad CRT-D models (OUS only); Implantable Cardioverter Defibrillators (ICDs) are implantable medical devices that automatically detect and treat episodes of ventricular fibrillation, ventricular tachycardia, fast ventricular tachycardia, and bradyarrhythmia. Some devices can also provide cardiac resynchronization therapy, including sequential biventricular pacing (CRT-D devices).

A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an earlier-than-expected RRT observation

ALL 50 STATES
Full report

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

Recall #:
87261
Lot/product code:
1) Viva family: MODEL NUMBER / NAME / GTIN: SERIAL NUMBERS BLF244376H, BLF243732H, BLF244567H, BLF243795H, BLF244186H, BLF244478H, BLF243894H, BLF243453H, BLF244610H, BLF244627H, BLF243514H, BLF242936H, BLF244189H, BLF243735H, BLF243429H, BLF244637H, BLF235234H, BLF242865H, BLF243129H, BLF243389H, BLF242685H, BLF243087H, BLF243671H, BLF243888H, BLF243897H, BLF244660H, BLF242664H, BLF242935H, BLF243975H, BLF243028H, BLF243445H, BLF243396H, BLF243947H, BLF243377H, BLF242659H, BLF244047H, BLF243393H, BLF243714H, BLF242861H, BLF243366H, BLF243378H, BLF242874H, BLF243382H, BLF243750H, BLF242082H, BLF242682H, BLF243363H, BLF243386H, BLF243413H, BLF243450H, BLF243452H, BLF243752H, BLF243513H, BLF243181H, BLF242551H, BLF243371H, BLF243772H, BLF241960H, BLF243455H, BLF243258H, BLF243391H, BLF243398H, BLF243401H, BLF243408H, BLF243055H, BLF244654H, BLF241810H, BLF242439H, BLF244207H, BLF243460H, BLF244390H, BLF241286H, BLF242713H, BLF242875H, BLF243142H, BLF243439H, BLF244165H, BLF242857H, BLF241855H, BLF243385H, BLF244651H, BLF242395H, BLF243179H, BLF242005H, BLF243442H, BLF244061H, BLF243397H, BLF242133H, BLF243010H, BLF243418H, BLF243435H, BLF243464H, BLF244080H, BLF240020H, BLF242060H, BLF242096H, BLF242674H, BLF242711H, BLF243068H, BLF243171H, BLF243430H, BLF243444H, BLF241170H, BLF244117H, BLF243086H, BLF243936H, BLF242691H, BLF243136H, BLF240023H, BLF242666H, BLF243941H, BLF243877H, BLF241596H, BLF242696H, BLF240265H, BLF241136H, BLF243474H, BLF240009H, BLF243059H, BLF243935H, BLF240016H, BLF241267H, BLF242876H, BLF241795H, BLF242444H, BLF243432H, BLF241869H, BLF243407H, BLF241846H, BLF242068H, BLF243808H, BLF243019H, BLF242260H, BLF243518H, BLF243506H, BLF244134H, BLF240017H, BLF242923H, BLF243089H, BLF240406H, BLF242391H, BLF242658H, BLF243096H, BLF240648H, BLF241838H, BLF241848H, BLF243495H, BLF240003H, BLF242405H, BLF242663H, BLF240032H, BLF241760H, BLF242324H, BLF242657H, BLF242707H, BLF244003H, BLF239398H, BLF240010H, BLF236242H, BLF240008H, BLF243030H, BLF243082H, BLF243479H, BLF243480H, BLF238259H, BLF238700H, BLF239843H, BLF242063H, BLF243447H, BLF240024H, BLF240547H, BLF242348H, BLF243056H, BLF243090H, BLF243105H, BLF239263H, BLF241473H, BLF242940H, BLF239773H, BLF240033H, BLF242708H, BLF243231H, BLF243667H, BLF238847H, BLF242209H, BLF240083H, BLF242680H, BLF242709H, BLF239264H, BLF242784H, BLF240503H, BLF243138H, BLF242471H, BLF243406H, BLF239866H, BLF241016H, BLF240879H, BLF241839H, BLF243034H, BLF243369H, BLF244112H, BLF243419H, BLF243708H, BLF241847H, BLF243405H, BLF243491H, BLF241851H, BLF242075H, BLF240794H, BLF241091H, BLF243424H, BLF239117H, BLF239889H, BLF242080H, BLF243976H, BLF244652H, BLF239615H, BLF242014H, BLF240857H, BLF243168H, BLF243791H, BLF240782H, BLF240830H, BLF242100H, BLF242779H, BLF243426H, BLF243449H, BLF243648H, BLF244128H, BLF244497H, BLF239864H, BLF242009H, BLF239244H, BLF239351H, BLF241853H, BLF241824H, BLF242007H, BLF242035H, BLF242204H, BLF242811H, BLF243511H, BLF233474H, BLF242026H, BLF242062H, BLF242910H, BLF243583H, BLF244009H, BLF238616H, BLF239587H, BLF240472H, BLF241836H, BLF241850H, BLF242024H, BLF242507H, BLF243373H, BLF243415H, BLF244508H, BLF239718H, BLF242021H, BLF242453H, BLF242808H, BLF243988H, BLF244500H, BLF242011H, BLF243955H, BLF244225H, BLF244573H, BLF240691H, BLF244431H, BLF242669H, BLF242817H, BLF244592H, BLF242008H, BLF238801H, BLF243255H, BLF235186H, BLF242114H, BLF242458H, BLF242877H, BLF238492H, BLF240026H, BLF239089H, BLF241043H, BLF241675H, BLF244655H, BLF243212H, BLF242249H, BLF243134H, BLF235187H, BLF236322H, BLF240612H, BLF239475H, BLF240856H, BLF241021H, BLF244471H, BLF244400H, BLF241010H, BLF243715H, BLF237913H, BLF238189H, BLF243062H, BLF244126H, BLF238047H, BLF243496H, BLF242066H, BLF239803H, BLF243857H, BLF244274H, BLF244562H, BLF236223H, BLF241307H, BLF242386H, BLF243473H, BLF243874H, BLF244381H, BLF244646H, BLF241843H, BLF244658H, BLF237433H, BLF238074H, BLF242735H, BLF235855H, BLF236051H, BLF242715H, BLF243294H, BLF243434H, BLF243274H, BLF241507H, BLF243198H, BLF243392H, BLF243505H, BLF243563H, BLF244312H, BLF241458H, BLF243451H, BLF243458H, BLF240776H, BLF244203H, BLF236843H, BLF236967H, BLF243061H, BLF237015H, BLF240254H, BLF240662H, BLF243612H, BLF241809H, BLF242334H, BLF242448H, BLF242812H, BLF244326H, BLF242901H, BLF243271H, BLF243652H, BLF244555H, BLF231669H, BLF235896H, BLF236939H, BLF238586H, BLF240895H, BLF243113H, BLF243762H, BLF241104H, BLF243525H, BLF243675H, BLF234586H, BLF238437H, BLF243388H, BLF243481H, BLF236549H, BLF239751H, BLF242896H, BLF243994H, BLF236965H, BLF243336H, BLF242639H, BLF235829H, BLF236571H, BLF241570H, BLF243423H, BLF244191H, BLF242221H, BLF244536H, BLF244159H, BLF238282H, BLF238845H, BLF238846H, BLF239749H, BLF234862H, BLF244276H, BLF235394H, BLF237489H, BLF243818H, BLF244071H, BLF235640H, BLF242889H, BLF243960H, BLF241297H, BLF239566H, BLF243687H, BLF244215H, BLF235675H, BLF240908H, BLF241314H, BLF241478H, BLF242645H, BLF243582H, BLF243906H, BLF241715H, BLF244467H, BLF233023H, BLF239304H, BLF2434… (truncated, 2884485 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 February 3, 2021

Implantable cardioverter defibrillators (ICD): 1) Evera family: Evera XT DR, Evera S DR, Evera MRI XT DR, Evera MRI S DR, Evera XT VR, Evera S VR and Evera MRI S VR models; 2) Visia family: Visia AF ICD, Visia AF S ICD, Visia AF MRI ICD, and Visia AF MRI S ICD models. Implantable Cardioverter Defibrillators (ICDs) are implantable medical devices that automatically detect and treat episodes of ventricular fibrillation, ventricular tachycardia, fast ventricular tachycardia, and bradyarrhythmia.

A small percentage of implanted cardiac devices, from a well-defined subset, may experience a shortened Recommended Replacement Time (RRT) to End of Service (EOS) interval following an earlier-than-expected RRT observation

ALL 50 STATES
Full report

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

Recall #:
87261
Lot/product code:
1) Evera Family: MODEL NUMBER / NAME / GTIN: SERIAL NUMBERS: DDBB1D1 / ICD-DR DDBB1D1 EVERA XT US IS1/DF1 / 00643169018099: BWC231766H, BWC230184H, BWC230891H, BWC228489H, BWC232037H, BWC230770H, BWC231219H, BWC231215H, BWC231190H, BWC231202H, BWC231199H, BWC231780H, BWC231556H, BWC230255H, BWC230772H, BWC230906H, BWC231500H, BWC231572H, BWC231618H, BWC231655H, BWC231937H, BWC231942H, BWC230859H, BWC230949H, BWC231848H, BWC230918H, BWC231237H, BWC231580H, BWC230893H, BWC231576H, BWC230426H, BWC230475H, BWC230431H, BWC231494H, BWC230876H, BWC230776H, BWC228873H, BWC229321H, BWC230873H, BWC229698H, BWC230449H, BWC231452H, BWC230877H, BWC230720H, BWC231479H, BWC231482H, BWC231578H, BWC231498H, BWC229796H, BWC230863H, BWC230874H, BWC231239H, BWC230917H, BWC229337H, BWC230524H, BWC230887H, BWC231525H, BWC231240H, BWC230672H, BWC230769H, BWC232164H, BWC232196H, BWC230048H, BWC230520H, BWC231568H, BWC231671H, BWC231761H, BWC229598H, BWC230335H, BWC230889H, BWC231570H, BWC228859H, BWC230914H, BWC231346H, BWC230884H, BWC231501H, BWC229058H, BWC229697H, BWC228813H, BWC232165H, BWC230870H, BWC230901H, BWC231259H, BWC230872H, BWC231106H, BWC230195H, BWC230911H, BWC228448H, BWC229342H, BWC230535H, BWC230655H, BWC230919H, BWC231269H, BWC231480H, BWC231668H, BWC230044H, BWC228426H, BWC230910H, BWC227091H, BWC231456H, BWC229099H, BWC229101H, BWC231874H, BWC228336H, BWC230869H, BWC230730H, BWC230630H, BWC231872H, BWC231343H, BWC228800H, BWC228656H, BWC228666H, BWC229097H, BWC231944H, BWC226887H, BWC230885H, BWC231768H, BWC232133H, BWC227119H, BWC228318H, BWC229963H, BWC230899H, BWC228760H, BWC230159H, BWC230882H, BWC230381H, BWC228544H, BWC230098H, BWC231400H, BWC228205H, BWC228858H, BWC226830H, BWC230454H, BWC228816H, BWC230608H, BWC228988H, BWC227088H, BWC228586H, BWC226816H, BWC227609H, BWC228180H, BWC228449H, BWC229289H, BWC229600H, BWC230118H, BWC230732H, BWC232122H, BWC231241H, BWC228818H, BWC229317H, BWC229344H, BWC229118H, BWC230071H, BWC227808H, BWC232126H, BWC232191H, BWC232170H, BWC227125H, BWC227610H, BWC227114H, BWC230530H, BWC227067H, BWC227782H, BWC228871H, BWC228399H, BWC228427H, BWC231659H, BWC228044H, BWC228820H, BWC228206H, BWC229013H, BWC231037H, BWC231809H, BWC226906H, BWC229163H, BWC227324H, BWC228320H, BWC227017H, BWC227077H, BWC227034H, BWC227374H, BWC228469H, BWC231485H, BWC225637H, BWC227113H, BWC228867H, BWC231257H, BWC227047H, BWC227071H, BWC224560H, BWC226819H, BWC226824H, BWC226960H, BWC227129H, BWC228864H, BWC230020H, BWC231332H, BWC231458H, BWC226403H, BWC226833H, BWC227056H, BWC227062H, BWC227126H, BWC228869H, BWC226939H, BWC227326H, BWC230083H, BWC231865H, BWC229346H, BWC231669H, BWC227323H, BWC230503H, BWC231049H, BWC228832H, BWC229536H, BWC226805H, BWC226822H, BWC226914H, BWC231406H, BWC228248H, BWC225448H, BWC226799H, BWC227109H, BWC228132H, BWC229168H, BWC231459H, BWC231673H, BWC226801H, BWC226817H, BWC228812H, BWC231043H, BWC231192H, BWC229055H, BWC226987H, BWC231173H, BWC229988H, BWC226820H, BWC226831H, BWC230642H, BWC226798H, BWC229516H, BWC229886H, BWC231781H, BWC226832H, BWC225279H, BWC226809H, BWC226812H, BWC227130H, BWC228297H, BWC229806H, BWC226664H, BWC230704H, BWC231684H, BWC226998H, BWC230322H, BWC225786H, BWC226298H, BWC227032H, BWC230010H, BWC231324H, BWC224500H, BWC229757H, BWC230573H, BWC227008H, BWC230091H, BWC231550H, BWC225592H, BWC226988H, BWC227163H, BWC227322H, BWC224540H, BWC230309H, BWC232166H, BWC227025H, BWC230791H, BWC231036H, BWC227845H, BWC230784H, BWC232050H, BWC226416H, BWC226966H, BWC228943H, BWC228960H, BWC228978H, BWC231908H, BWC228014H, BWC228050H, BWC229537H, BWC226984H, BWC227330H, BWC231176H, BWC231412H, BWC229009H, BWC230481H, BWC226584H, BWC229898H, BWC225730H, BWC226415H, BWC226924H, BWC227316H, BWC227321H, BWC230411H, BWC226578H, BWC229981H, BWC230279H, BWC224159H, BWC225056H, BWC230137H, BWC229606H, BWC231774H, BWC225810H, BWC226471H, BWC227919H, BWC228962H, BWC229743H, BWC230565H, BWC228743H, BWC231660H, BWC225960H, BWC228522H, BWC232106H, BWC232113H, BWC225555H, BWC227536H, BWC228919H, BWC228974H, BWC208701H, BWC231047H, BWC226182H, BWC231976H, BWC226398H, BWC226639H, BWC229914H, BWC230318H, BWC230916H, BWC230937H, BWC231395H, BWC232174H, BWC226053H, BWC228270H, BWC225617H, BWC226923H, BWC228131H, BWC229142H, BWC230648H, BWC231137H, BWC224556H, BWC224377H, BWC225611H, BWC226587H, BWC228342H, BWC229758H, BWC230247H, BWC230404H, BWC224492H, BWC228171H, BWC228363H, BWC228582H, BWC229921H, BWC230590H, BWC230691H, BWC231024H, BWC231250H, BWC231392H, BWC232118H, BWC232181H, BWC222232H, BWC223575H, BWC226139H, BWC226703H, BWC227005H, BWC227196H, BWC228392H, BWC228969H, BWC229071H, BWC229414H, BWC230028H, BWC230181H, BWC231490H, BWC231729H, BWC231864H, BWC231997H, BWC232155H, BWC232206H, BWC225667H, BWC226056H, BWC226643H, BWC231184H, BWC232115H, BWC226299H, BWC227028H, BWC228060H, BWC227023H, BWC228445H, BWC229075H, BWC229787H, BWC232001H, BWC220805H, BWC225084H, BWC227612H, BWC227882H, BWC228414H, BWC230410H, BWC230774H, BWC231403H, BWC231549H, … (truncated, 3486040 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 February 3, 2021

Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid disorders (such as diabetes mellitus), various liver and renal diseases, and in the assessment of risk for atherosclerosis and cardiovascular disease.

Siemens Healthcare Diagnostics Inc. has confirmed the potential for erroneous results due to discolored reagent observed in some wells 5 and 6 of Dimension Vista High Density Lipoprotein Cholesterol (HDLC) Flex reagent cartridges lot 20062BA.

ALL 50 STATES
Full report

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

Recall #:
87319
Lot/product code:
Product: DV HDLC; Lot #: 20062BA; UDI Number: 0084276802043820062BA21030210464340840
Recalling firm:
Siemens Healthcare Diagnostics, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 4, 2021

Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

The ultrasound system averages the Mean Sac Diameter (MSD) and Gestational Sac Diameter (GSD) into the Estimated Date of Delivery (EDD) calculation. This may result in an incorrect EDD, which may influence patient management decisions regarding induction of labor and elective caesarean delivery, which may result in premature births.

Full report

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

Recall #:
87362
Lot/product code:
Model: 11148775  Equipment Serial Numbers (U.S.) 800015 800101 800103 800104 800105 800106 800107 800108 800109 800111 800112 800113 800116 800118 800119 800121 800134 800138 800139 800141 800142 800143 800149 800150 800151 800152 800153 800155 800157 800158 800161 800165 800168 800172 800174 800175 800176 800177 800178 800182 800183 800184 800185 800186 800189 800190 800191 800192 800193 800194 800195 800196 800198 800199 800201 800203 800204 800205 800208 800209 800210 800211 800215 800217 800220 800221 800223 800225 800226 800227 800228 800229 800232 800233 800234 800235 800237 800239 800241 800242 800243 800244 800247 800249 800251 800254 800256 800257 800258 800259 800260 800263 800265 800267 800268 800270 800273 800274 800278 800280 800281 800285 800286 800291 800292 800293 800295 800300 800301 800302 800303 800304 800305 800308 800313 800314 800317 800319 800320 800321 800324 800328 800333 800335 800336 800339 800341 800342 800348 800349 800355 800360 800361 800363 800366 800369 800370 800375 800376 800383 800390 800393 800397 800405 800408 800411 800418 800424 800427 800428 800429 800433 800435 800436 800440 800451 800462 800463 800464 800466 800467 800469 800473 800474 800475 800480 800481 800486 800489 800490 800495 800498 800505 800506 800509 800511 800515 800516 800518 800521 800523 800525 800528 800532 800535 800540 800546 800549 800550 800552 800555 800556 800559 800560 800564 800566 800567 800579 800581 800583 800590 800592 800594 800597 800598 800607 800609 800611 800618 800623 800627 800628 800630 800631 800634 800638 800639 800640 800645 800648 800650 800651 800652 800653 800657 800661 800662 800667 800668 800671 800672 800673 800674 800675 800677 800680 800683 800686 800688 800693 800694 800696 800701 800703 800707 800708 800735 800738 800739 800741 800742 800743 800745 800747 800749 800752 800754 800756 800758 800760 800761 800762 800763 800771 800775 800786 800787 800788 800789 800791 800800 800805 800806 800807 800809 800813 800821 800834 800835 800854 800859 800861 800862 800863 800865 800866 800868 800869 800870 800871 800873 800874 800876 800878 800879 800880 800881 800882 800883 800884 800885 800887 800889 800890 800896 800901 800903 800904 800906 800907 800908 800912 800913 800914 800915 800917 800918 800920 800931 800933 800936 800940 800944 800945 800947 800952 800955 800959 800961 800963 800964 800979 800980 800993 800994 800998 801002 801003 801004 801005 801006 801007 801008 801009 801010 801011 801013 801014 801015 801016 801017 801018 801019 801021 801022 801023 801025 801026 801033 801034 801047 801080 801084 801087 801088 801089 801116 801117 801121 801123 801124 801125 801126 801127 801128 801129 801130 801131 801133 801134 801135 801136 801137 801138 801139 801140 801141 801144 801145 801147 801150 801152 801153 801156 801165 801166 801174 801177 801178 801191 801192 801193 801194 801196 801200 801202 801209 801211 801213 801223 801225 801230 801232 801234 801244 801245 801247 801248 801249 801259 801261 801271 801278 801279 801286 801300 801302 801306 801310 801311 801313 801314 801315 801316 801321 801324 801325 801326 801328 801330 801334 801336 801339 801345 801346 801347 801348 801352 801353 801356 801357 801358 801360 801363 801365 801366 801371 801372 801378 801381 801386 801390 801396 801400 801402 801405 801406 801408 801413 801414 801421 801423 801424 801426 801427 801430 801432 801435 801436 801437 801439 801441 801442 801443 801444 801447 801449 801450 801451 801452 801454 801458 801462 801463 801464 801465 801470 801471 801473 801474 801475 801476 801481 801483 801484 801488 801491 801492 801494 801495 801497 801499 801501 801502 801503 801506 801509 801510 801514 801515 801516 801517 801519 801521 801524 801527 801528 801529 801530 801531 801532 801534 801535 801536 801537 801538 801539 801540 801541 801542 801543 801544 801545 801548 801549 801550 801552 801553 801554 801555 801556 801558 801559 801564 801565 801567 801572 801574 801576 801579 801594 801596 801598 801605 801609 801610 801611 801629 801631 801632 801636 801639 801641 801642 801643 801645 801647 801648 801649 801650 801655 801660 801663 801675 801678 801680 801685 801708 801714 801759 801760 801768 801771 801812 801903 801911 802004 802008 802017 802019 802022 802028 802029 802032 802033 802093 802109 802125 802128 802146 802164 802217 802245 802263  Equipment Serial Numbers (O.U.S.): 800344 800438 800932 801787 801851 801020 801927 801982 801988 802069 802073 802078 802079 802081 802083 802084 802086 802123 802131 802135 802140 802147 802180 802181 802183 802185 802186 802187 802188 802189 800114 800115 800117 800120 800122 800123 800126 800127 800129 800130 800133 800135 800136 800140 800147 800148 800159 800162 800163 800166 800167 800169 800170 800171 800181 800187 800197 800206 800207 800212 800214 800218 800219 800224 800230 800231 800236 800245 800246 800248 800250 800252 800264 800266 800271 800277 800279 800282 800284 800288 800298 800309 800311 800312 800315 800323 800329 800334 8… (truncated, 8288 characters total — see the official FDA record for the full value)
Recalling firm:
Siemens Medical Solutions USA, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 5, 2021

System INFX-8000V

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

ALL 50 STATES
Full report

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

Recall #:
87419
Lot/product code:
Model: CAS-880A, CAS-830B
Recalling firm:
Canon Medical System, USA, INC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 5, 2021

System INFX-8000F

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

ALL 50 STATES
Full report

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

Recall #:
87419
Lot/product code:
Model: CAS-880A, CAS-830B
Recalling firm:
Canon Medical System, USA, INC.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled February 5, 2021

System INFX-8000C

The x-ray irradiation field may shift with respect to image receiving surface displayed on the screen at some C-arm angles.

ALL 50 STATES
Full report

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

Recall #:
87419
Lot/product code:
Model: CAS-880A, CAS-830B
Recalling firm:
Canon Medical System, USA, INC.
View official FDA record (opens in a new tab)