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Recalls affecting Illinois

Data last updated: September 8, 2026 at 1:13 PM UTC

17,357 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/virusAnnounced 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/virusAnnounced 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)
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)
UnclassifiedAllergenUndeclaredAnnounced 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)
UnclassifiedBacteria/virusAnnounced 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/virusAnnounced 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 May 14, 2026

ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS12-120LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS12-120LPI. UDI-DI: 10845854045688. Lot Numbers: 202506164, 202507144, 202506274, 202506136, 202506124, 2025071010, 202507114, 202506244, 202505194, 202505164, 202505064, 202505144, 202509114, 202508204, 202509124, 202510184, 202509274, 202511064, 202509254, 202509264, 202510254, 202510274, 202508294, 202509104, 202508214, 202509154, 202508084, 202507264, 202507254, 2025080611, 202507284, 202512124, 202511204, 202511214, 202511244, 202512134, 2025100310, 202510034, 202510154, 202511065, 202511075, 202511074, 202510244, 202510174, 202502214, 202503204, 202503075, 202503064, 202504244, 202504025, 2025040310, 2025040411, 202504046, 202503215, 202503244, 202504044, 202501164, 202501244, 202501235, 202506134, 202406204, 202406245, 202408154, 202502194, 202501145, 202505054, 202504036, 202412134, 202501274, 202408095, 202407316, 202410305, 202410244, 202506254, 202508274, 202509244, 202410234, 202411045, 202409035, 202407106, 202506304, 202512104, 202510204, 202501225, 202406214, 2025040210, 2025042110, 2025080810, 202508264, 202408135, 202410315, 202410295, 202408214, 202408294, 202507234, 202505304, 202505294, 202407155, 202408204, 202408206, 202406195, 202503065, 202502244, 202501095, 202504305, 202511086, 2024111911, 202501144, 2025110410, 2025110510, 202510164, 202511104, 2025122310, 202504304, 202501166, 202502184, 202407104, 202406215, 202406206, 202506264, 202410255, 202508284, 202507244, 202408015, 202505154, 202407305, 202411236, 2024112210, 202412105, 2025110512, 202501224, 202512154, 202407114, 202504294, 2025111910, 202407105, 202406266, 202501104, 202501275, 202503086, 2025040211, 2025111810, 2025041610, 2025110511, 202411054, 202408164, 202507104, 202408065, 202501286, 202503114, 202503214, 202412235, 202506024, 2024112111, 2024112010, 202505274, 202410304, 202411015, 202410225, 202408125, 202408205, 202409034, 202408165, 202510035, 202408155, 202408296, 202407154, 202407124, 202408064, 202406284, 202406205, 202601064, 2025122210, 2025111410, 202511066, 202411265, 202411225, 202411224, 202506104, 202408176, 202410294, 202512234, 202407015, 202407014, 202407125, 202504224, 202505014, 202411195, 202502064, 202411014, 202408094, 202411216, 202411214, 202504214, 202507094, 202406285, 202406244, 202502205, 202503205, 2024112610, 202412144, 202410235, 202411255, 202501246, 202408106, 202408224, 202407254, 202407024, 202504056, 202503245, 202501245, 202502075, 202501234, 202502114, 2024112011, 202411206, 202412135, 202406275, 202501024, 202411276, 202412124, 2024112211, 2024121210, 2025102310, 202512114, 202601055, 2025080710, 202506114, 202505284, 202505176, 202407314, 202408144, 202408134, 202410245, 202411194, 202411254, 2024121310, 202501025, 202501155, 202412114, 202408084, 202501086, 202502204, 202501034, 202412226, 202406254, 202509014, 2025100210, 202511076, 202503195, 202412164, 202407256, 202407116, 202411226, 202406286, 202407136, 202408194, 2025081110, 202411205, 202408146, 202411264, 202412234, 202411215, 202406226, 2025040710, 202501256, 202502055, 202410314, 202410284, 202408295, 202408145, 202408136, 202501154, 202502105, 202501236, 202411266, 202408124, 2024121311, 202503105, 2025040311, 202406255, 202407095, 202412125, 2024112510, 2025043010, 2024112110, 2024112511, 202408156, 202501226, 202408216, 202501085, 202407026, 2026010511, 2024071212, 202407126, 202410285, 202408166, 202406256, 202504174, 2024121211. OUS added 06/10/2026 expansion: 202411204, 202511075, 202511244, 202509154, 202509104, 202509264, 202508084, 2025080611, 202507284, 202507254, 202507264, 202504174, 202506274, 2025040310, 202504244, 202505144, 202501085, 202501094, 202504164, 202502214, 2024112110, 202410245, 202410285, 202411044, 2024112011, 202412105, 202411266, 202510274, 202510184, 202406226, 202406216, 202407024, 202407136, 202408066, 2024071212, 202511064, 202511065, 202509274, 202508214, 202510254, 202506124, 202503204, 202504044, 202505064, 202503075, 202501244, 202501154, 202407026, 202408194, 202407116, 202511214, 2025071010, 202505164, 202410315, 202501166, 202512124, 202408304, 202410225, 202408135, 202511074, 202509124, 202510244, 2025100310, 202507144, 202505194, 2025041710, 202501084, 202406255, 202407126, 202408195, 202411214, 202408084, 202508204, 2025040410, 202411225, 202509114, 202503064, 202406256, 202407245, 202412124, 202511204, 202509254, 202510154, 202510034, 202504046, 2025040411, 202501235, 202501256, 202510035, 202512154, 202503065, 202407105, 202408144, 202506114, 202510204, 202512114, 202503245, 202501034, 202501224, 202411215, 202507244, 202509014, 202509244, 202508284, 202511086, 202511104, 202601064, 2024121210, 202408216, 202412234, 202502114, 202504056, 202411194, 2025043010, 202506134, 202507114, 202406245, 202408164, 2025080810, 202409034, 202508264, 202406214, 202408295, 202410294, 202504304, 202506164, 202506304, 202502105, 2024121311, 202410305, 202408146, 202504214, 202501164, 202601124, 202507234, 2025041610, 202501145, 202410284, 202408064, 202408136, 2024… (truncated, 5684 characters total — see the official FDA record for the full value)
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS8-120LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS8-120LP. UDI-DI: 10845854045657. Lot Numbers: 202503274, 202503314, 202504254, 2025100710, 2025092210, 2025100810, 2025092610, 202510164, 202511204, 2025102410, 2025111210, 202506124, 202506136, 202506164, 202507234, 202507104, 202507114, 202509054, 202407054, 202410245, 202409196, 202503185, 202408295, 202407084, 202501084, 202511285, 202511214, 202412185, 202501175, 202505134, 202502226, 202406185, 202407255, 202407044, 202406195, 202510174, 202508204, 202507094, 202411154, 202410185, 202407175, 202411044, 202411155, 202508114, 202506115, 202505124, 202508234, 202406265, 202501204, 202501226, 202501275, 202505214, 202511244, 202410305, 202409205, 202409206, 202507014, 202505314, 202509044, 2025082510, 202502204, 2025112610, 202502065, 202508194, 202504244, 202407155, 202409194, 202407034, 202410294, 202411065, 202407154, 202508084, 202506304, 2025100610, 2025102710, 2025111410, 202503284, 202407025, 202407225, 202408205, 202409065, 202407234, 202510304, 202508064, 202508074, 202506134, 202411055, 202505264, 202508214, 2025111310, 2025090410, 202511284, 202510204, 202410214, 202501256, 202407115, 202406254, 202409044, 202504284, 202501284, 202503264, 202407235, 202410304, 202505304, 202509264, 202411145, 202410184, 202501074, 202407264, 2025090210, 202507224, 202410215, 202409064, 202511014, 2025082310, 202507264, 202511224, 202509254, 2025091910, 2025101310, 202407055, 202407185, 202505224, 202502104, 202501215, 202410225, 202502286, 202501285, 202504114, 202407174, 202407125, 202407165, 202406255, 202407124, 202406275, 202406264, 202407244, 202408074, 202407164, 202503296, 202504094, 202503315, 202502284, 202502206, 202502076, 202505084, 202504144, 202512054, 2025112510, 202510314, 202512014, 2025102510, 202411274, 202411144, 202411275, 202501165, 202501116, 202501095, 202501164, 202502075, 202411064, 202410224, 202501106, 2025101010, 2025090510, 202511134, 2025092710, 202508224, 2025091210, 2025090310, 202411134, 202411045, 202411125, 202411284, 202411135, 202409076, 202409234, 202410285, 202507284, 2025081912, 202506024, 202506126, 202507144, 202501214, 202410295, 202411265, 2025101110, 202510184, 2026010810, 202406274, 202407184, 202505234, 202409054, 202409204, 202407045, 202407305, 202407114, 202406175, 202511034, 202502285, 202507084, 202509274, 202411285, 202406174, 202504164, 202511264, 202408195, 202409055, 202407035, 202409216, 202504104, 202502214, 202406144, 202501105, 202501205, 2025100910, 202501104, 2025091810, 202407304, 202406194, 202408204, 202502064, 2025090810, 202410145, 202503184, 202501075, 202505236, 202502205, 202411184, 202510315, 202502086, 202407265, 202507214, 2025081810, 202409185, 202409195, 202408285, 202406184, 202407314, 202409184, 202502216, 202505074, 202407245, 202411185, 202503146, 202502275, 202502215, 202410284, 202512084, 202408294, 202410144, 202412194, 2026010710, 202501216, 2025092010, 202411124, 2025090910, 202411054, 202409045, 202407295, 2025092600, 202407024, 202408214, 202407315, 202412136. OUS added 06/10/2026 expansion: 2025100810, 2025100710, 202511204, 2025092610, 202506124, 202411285, 202507114, 202505234, 202503314, 202501164, 202410304, 202410305, 202407294, 202409065, 202507224, 202406195, 202501104, 202501084, 202411054, 202410295, 202407314, 2025102410, 202510164, 202501205, 202507104, 202506164, 202504254, 202407034, 202506136, 202503274, 202409206, 2025092210, 202511264, 202508234, 202507094, 202508084, 202508224, 202505224, 202504094, 202506134, 202502204, 202502206, 202501275, 202408204, 202501074, 202412185, 202409076, 202407025, 202406174, 202407054, 202407114, 202409064, 202505124, 202411044, 202501075, 202410225, 202511214, 2025100610, 202507264, 2025100910, 202411265, 202508214, 202407185, 202411055, 202407164, 202407165, 202504164, 202510204, 202509054, 202502064, 2025111210, 202509044, 202410145, 202505236, 202512054, 2025090410, 202505304, 202505134, 202501116, 202409055, 202511284, 2025091910, 2025090310, 202501284, 202407255, 202504284, 202507234, 202505214. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 12 mm Access Port and Obturator with Blunt Tip, 120mm Length. Catalog Number: iASB12-120. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iASB12-120. UDI-DI: 10845854045725. Lot Numbers: 202507314, 202506194, 202510024, 202501165, 202504034, 202408225, 202411264. OUS added 06/10/2026 expansion: 202510024, 202507314, 202504034, 202501165, 202411264, 202408225, 202506194. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 8mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 100mm Length. Catalog Number: iAS8-100LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS8-100LP. UDI-DI: 10845854045718. Lot Numbers: 202509034, 202511194, 202509174, 202506264, 202506254, 202506274, 202507074, 202505096, 202507244, 202508124, 202508194, 202507084, 202504294, 202505074, 202504304, 202504155, 202505064, 202505094, 202505204, 202509244, 202511184, 2025102210, 202508254, 2025111110, 202510154, 202508054, 202508114, 202507254, 202509084, 202509054, 202411015, 202408155, 202503016, 202504234, 202505264, 202501134, 202411124, 202501135, 202412195, 202411305, 202511274, 202509274, 202511284, 202504284, 202504224, 202503194, 202504085, 202508184, 202510304, 202409034, 202409095, 202409094, 202408085, 202410104, 202506304, 202506054, 202510094, 202409025, 202410175, 202508264, 202408095, 202408125, 202411115, 202411014, 202506044, 202509194, 202511264, 202408274, 202412205, 202412025, 202501236, 202501235, 202501244, 202503156, 202503145, 202503144, 202504084, 202408094, 202408084, 202410105, 202502066, 202501094, 202509184, 202408275, 202408194, 202507144, 202507154, 202412024, 202501234, 202411295, 202504094, 202503196, 202503125, 202503126, 202503034, 202504145, 202408165, 2025081811, 202408154, 202503264, 202502055, 202411294, 202412106, 202601074, 2026010711, 202501225, 202412204, 202501245, 202409106, 202410315. OUS added 06/10/2026 expansion:202408284, 202509244, 202507254, 202508054, 202508194, 202505064, 202504294, 202504155, 202504304, 202501085, 202501146, 202501274, 202501224, 202410314, 202410315, 202509034, 2025111110, 202509174, 202507244, 202508124, 202506274, 202505204, 202506254, 202503144, 202409106, 202511184, 202505096, 202501225, 202510154, 202408165, 202508114, 202508254, 202408085, 202507084, 202505094, 202507074, 202503194, 202501135, 202412205, 202412204, 202408084, 202411295, 202412106, 202509054, 202509084, 2025102210, 202504084, 202503196, 202504145, 202501094, 202408164, 202411124, 202503125, 202408094, 202505074, 202504224, 202411294, 202507144, 202408095, 202506304, 202511274, 202508184, 202503264, 202411115, 202504234, 202506264, 202501244, 202503034, 202509184, 202501236, 202411305, 202510304, 202505264, 202502055, 202412025, 202412195, 202410175, 202506054, 2025081811, 202503016, 202409034, 202409094, 202501134, 202507154, 202511284, 202506044, 202510094, 202411015, 202503145, 202408274, 202511264, 202411014, 202408155, 202509274, 202503156, 202508264, 202408194, 202504094, 202501234, 202408275, 202408154, 202408075, 202511194, 202504085, 202501245, 202412024, 202410115, 202412126, 202409025, 202409095, 202501235, 202410104. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 12mm Access Port and Obturator with Blunt Tip, 100mm Length. Catalog Number: iASB12-100. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iASB12-100. UDI-DI: 10851885004310. Lot Numbers: 202510034, 202505134, 202507234, 202510094, 202503184, 202408306, 202407044, 202412194, 202512014, 202512024, 202410085, 202411264. OUS added 06/10/2026 expansion: 202510034, 202412194, 202411264, 202503184, 202410085, 202507234, 202408306, 202407044, 202505134, 202512024, 202512014, 202510094. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 5 mm Smooth Access Port and Obturator with Blunt Tip, 150mm Length. Catalog Number: iASB5-150. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iASB5-150. UDI-DI: 10845854045695. Lot Numbers: 202510144, 202508124, 202501144, 202408144, 202412044, 202505064, 202511284. OUS added 06/10/2026 expansion: 202408144, 202501144, 202505064, 202508124, 202510144. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS12-150LPI. UDI-DI: 10845854052006. Lot Numbers: 202509234, 202506104, 202505074, 202503204, 202510094, 202510144, 202508194, 202506244, 202512054, 202512234, 202511224, 202504164, 202504074, 202407294, 202511214, 202410254, 202512184, 202412175, 202407115, 202411055, 202411284, 202408235, 202411274, 202502275. OUS added 06/10/2026 expansion: 202510144, 202510094, 202506244, 202509234, 202504074, 202412175, 202408235, 202407294, 202508194, 202410254, 202408234, 202503204, 202506104, 202411055, 202505074, 202504164, 202512184, 202411274, 202511224, 202511214, 202601124, 202502275, 202411284, 202512054, 202407115. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

Automated Impella Controller (AIC), for use with left heart support blood pump. Labeled as the following with corresponding Product Codes: 1. Impella Controller, Packaged, AU; Product Code: 0042-0000-AU. 2. Impella Controller, Packaged, CA; Product Code: 0042-0000-CA. 3. Impella Controller, Packaged, EU; Product Code: 0042-0000-EU. 4. Impella Controller, Packaged, IN; Product Code: 0042-0000-IN. 5. Impella Controller, Packaged, JP; Product Code: 0042-0000-JP. 6. Impella Controller, Packaged, UK; Product Code: 0042-0000-UK. 7. Impella Controller, Packaged, US; Product Code: 0042-0000-US. 8. Impella Optical Controller, Packaged, AU; Product Code: 0042-0010-AU. 9. Impella Optical Controller, Packaged, EU; Product Code: 0042-0010-EU. 10. Impella Optical Controller, Packaged, IN; Product Code: 0042-0010-IN. 11. Impella Optical Controller, Packaged, UK; Product Code: 0042-0010-UK. 12.Impella Optical Controller, Packaged, US, UK; Product Code: 0042-0010-US. 13. Optical AIC w/Impella Connect, Pack'd, CA; Product Code: 0042-0040-CA. 14. Optical AIC w/Impella Connect, Pack'd, EU; Product Code: 0042-0040-EU. 15. Optical AIC w/Impella Connect, Pack'd, JP, EU; Product Code: 0042-0040-JP. 16. Optical, AIC, Impella Connect, Pkgd, AU; Product Code: 0042-0040-AU. 17. Optical, AIC, Impella Connect, Pkgd, UK; Product Code: 0042-0040-UK. 18. Optical, AIC, Impella Connect, Pkgd, US; Product Code: 0042-0040-US.

Potential software error in the Automated Impella Controller ("AIC" ) when used in conjunction with left ventricular Impella devices.

ALL 50 STATES
Full report

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

Recall #:
98853
Lot/product code:
All products below with software versions 6.0.1, 6.0.2, 6.0.3, 7.1 and above. 1. Product Code: 0042-0000-AU; GTIN: 00813502010886; Serial Numbers: IC5341, IC5523, IC5677, IC6531, IC5525, IC6529, IC5836, IC5524, IC7849, IC7850, IC7287, IC7288, IC7289, IC7290, IC6527, IC6526, IC6528, IC6530, IC5622, IC5752, IC5521, IC5522, IC5217, IC5216. 2. Product Code: 0042-0000-CA; GTIN: 00813502011272; Serial Numbers: IC9415, IC9413, IC9416, IC9414, IC8283, IC7716, IC7695, IC7694, IC6635, IC6636, IC6633, IC6634, IC6082, IC6083, IC5821, IC5824, IC5680, IC3802, IC2035, IC1912, IC5034, IC5050, IC4944, IC4945, IC3803, IC3661, IC3662, IC2686, IC2687, IC2033, IC1913, IC1790, IC1791, IC1911, IC1715, IC1769, IC1664, IC1595, IC1598, IC1543, IC1480, IC1481, IC1324, IC1346. 3. Product Code: 0042-0000-EU; GTIN: 00813502011289; Serial Numbers: IC7809, IC7720, IC7721, IC7748, IC7719, IC7718, IC7717, IC7691, IC7692, IC7693, IC7689, IC7690, IC7687, IC7688, IC7675, IC7686, IC7674, IC7667, IC7655, IC7666, IC7647, IC7648, IC7649, IC7650, IC7651, IC7652, IC7646, IC7653, IC7654, IC7613, IC7614, IC7615, IC7580, IC7578, IC7579, IC7576, IC7577, IC7421, IC7455, IC7407, IC7395, IC7406, IC7393, IC7394, IC7388, IC7389, IC7390, IC7392, IC7378, IC7286, IC7265, IC7263, IC7264, IC7261, IC7262, IC7258, IC7259, IC7260, IC7098, IC7099, IC7100, IC7078, IC7093, IC7087, IC7092, IC7096, IC7097, IC7094, IC7095, IC7077, IC7075, IC7076, IC6880, IC6876, IC6877, IC6878, IC6879, IC6845, IC6843, IC6813, IC6814, IC6810, IC6812, IC6804, IC6805, IC6806, IC6807, IC6808, IC6809, IC6716, IC6717, IC6728, IC6738, IC6739, IC6740, IC6741, IC6742, IC6713, IC6714, IC6710, IC6712, IC6711, IC6715, IC6708, IC6709, IC6594, IC6595, IC6688, IC6689, IC6690, IC6691, IC6692, IC6693, IC6694, IC6695, IC6706, IC6707, IC6591, IC6592, IC6593, IC6579, IC6577, IC6578, IC6587, IC6588, IC6589, IC6590, IC6582, IC6580, IC6581, IC6534, IC6535, IC6536, IC6487, IC6488, IC6449, IC6469, IC6441, IC6443, IC6440, IC6436, IC6437, IC6439, IC6432, IC6435, IC6434, IC6431, IC6331, IC6270, IC6064, IC6205, IC6275, IC6273, IC6274, IC6225, IC6236, IC6272, IC6223, IC6224, IC6149, IC6150, IC6151, IC6147, IC6081, IC6078, IC5818, IC5817, IC5781, IC5775, IC5777, IC5779, IC5755, IC5756, IC5754, IC5715, IC5716, IC5717, IC5685, IC5686, IC5611, IC5714, IC5722, IC5683, IC5684, IC5688, IC5560, IC5681, IC5682, IC5559, IC5518, IC5520, IC5517, IC5177, IC4839, IC4565, IC5519, IC5495, IC5496, IC5494, IC5490, IC5491, IC5492, IC5493, IC5487, IC5488, IC5476, IC5477, IC5460, IC5461, IC5463, IC5464, IC5462, IC5443, IC5441, IC5442, IC5440, IC5435, IC5436, IC5433, IC5434, IC5331, IC5356, IC5421, IC5422, IC5391, IC5392, IC5252, IC5195, IC5048, IC5193, IC5194, IC5178, IC5175, IC5176, IC5173, IC5174, IC5210, IC5212, IC5171, IC5169, IC5086, IC5051, IC5053, IC5075, IC5057, IC5087, IC5088, IC5046, IC5047, IC5049, IC5008, IC5009, IC4973, IC5007, IC4984, IC4986, IC4987, IC4988, IC4933, IC4934, IC4931, IC4932, IC4850, IC4928, IC4929, IC4930, IC4623, IC4470, IC4912, IC4917, IC4913, IC4915, IC4914, IC4916, IC4846, IC4837, IC4833, IC4834, IC4835, IC4836, IC4823, IC4824, IC4821, IC4822, IC4845, IC4840, IC4819, IC4820, IC4817, IC4818, IC4815, IC4816, IC4796, IC4797, IC4792, IC4793, IC4794, IC4795, IC4763, IC4790, IC4791, IC4781, IC4762, IC4760, IC4761, IC4758, IC4759, IC4748, IC4757, IC4737, IC4738, IC4735, IC4736, IC4733, IC4734, IC4723, IC4724, IC4728, IC4729, IC4725, IC4727, IC4679, IC4680, IC4677, IC4678, IC4657, IC4658, IC4648, IC4649, IC4646, IC4647, IC4645, IC4656, IC4634, IC4635, IC4636, IC4632, IC4633, IC4630, IC4631, IC4585, IC4629, IC4626, IC4624, IC4627, IC4613, IC4614, IC4611, IC4569, IC4566, IC4568, IC4610, IC4612, IC4609, IC4597, IC4598, IC4557, IC4567, IC4594, IC4595, IC4559, IC4564, IC4560, IC4561, IC4562, IC4563, IC4505, IC4506, IC4508, IC4501, IC4471, IC4500, IC4469, IC4466, IC4467, IC4464, IC4465, IC4468, IC4442, IC4443, IC4444, IC4445, IC4446, IC4370, IC4371, IC4367, IC4365, IC4366, IC4361, IC4359, IC4360, IC4358, IC4329, IC4328, IC4234, IC4362.IC4363, IC4356, IC4357, IC4323, IC4324, IC4325, IC4326, IC4322, IC4258, IC4252, IC4253, IC4251, IC4242, IC4241, IC4240, IC4254, IC4255, IC4256, IC4235, IC4238, IC4236, IC4230, IC4227, IC4228, IC4229, IC4210, IC4212, IC4207, IC4208, IC4218, IC4217, IC4209, IC4211, IC4175, IC4153, IC4151, IC4152, IC4150, IC4146, IC4147, IC4148, IC4149, IC4128, IC4129, IC4099, IC4100, IC4096, IC4097, IC4098, IC4083, IC4081, IC4036, IC4037, IC4034, IC4035, IC4033, IC4002, IC4006, IC4012, IC4013, IC4014, IC4015, IC3891, IC3889, IC3866, IC3867, IC3868, IC3869, IC3859, IC3861, IC3833, IC3834, IC3862, IC3863, IC3885, IC3886, IC3884, IC3870, IC3871, IC3872, IC3873, IC3874, IC3864, IC3860, IC3832, IC3830, IC3831, IC3828, IC3829, IC3815, IC3816, IC3777, IC3817, IC3818, IC3813, IC3814, IC3781, IC3782, IC3780, IC3812, IC3778, IC3724, IC3718, IC2710, IC3717, IC3706, IC3707, IC3708, IC3701, IC3703, IC3709, IC3698, IC3702, IC3699, IC3700, IC3697, IC3696, IC3673, IC3671, IC3672, IC3668, IC3670, IC3657, IC3669, IC3667, I… (truncated, 86374 characters total — see the official FDA record for the full value)
Recalling firm:
Abiomed, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 5mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 75mm Length. Catalog Number: iAS5-75LP. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS5-75LP. UDI-DI: 10845854046388. Lot Numbers: 202509294, 202508044, 202505144, 202504014, 202502275, 202512034, 202507014, 202510084, 202412144, 202411065, 202409305, 202406284, 202408014, 202409304, 202506254. OUS added 06/10/2026 expansion: 202502275, 202509294, 202504014, 202507014, 202505144, 202512034, 202411065, 202508044, 202409305, 202409304, 202408014, 202506254, 202510084, 202412144, 202406284. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 12mm Access Port and Low Profile Obturator with Bladeless Optical Tip, 120mm Length. Catalog Number: iAS12-120LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS12-120LPI. UDI-DI: 10845854045688. Lot Numbers: 202506164, 202507144, 202506274, 202506136, 202506124, 2025071010, 202507114, 202506244, 202505194, 202505164, 202505064, 202505144, 202509114, 202508204, 202509124, 202510184, 202509274, 202511064, 202509254, 202509264, 202510254, 202510274, 202508294, 202509104, 202508214, 202509154, 202508084, 202507264, 202507254, 2025080611, 202507284, 202512124, 202511204, 202511214, 202511244, 202512134, 2025100310, 202510034, 202510154, 202511065, 202511075, 202511074, 202510244, 202510174, 202502214, 202503204, 202503075, 202503064, 202504244, 202504025, 2025040310, 2025040411, 202504046, 202503215, 202503244, 202504044, 202501164, 202501244, 202501235, 202506134, 202406204, 202406245, 202408154, 202502194, 202501145, 202505054, 202504036, 202412134, 202501274, 202408095, 202407316, 202410305, 202410244, 202506254, 202508274, 202509244, 202410234, 202411045, 202409035, 202407106, 202506304, 202512104, 202510204, 202501225, 202406214, 2025040210, 2025042110, 2025080810, 202508264, 202408135, 202410315, 202410295, 202408214, 202408294, 202507234, 202505304, 202505294, 202407155, 202408204, 202408206, 202406195, 202503065, 202502244, 202501095, 202504305, 202511086, 2024111911, 202501144, 2025110410, 2025110510, 202510164, 202511104, 2025122310, 202504304, 202501166, 202502184, 202407104, 202406215, 202406206, 202506264, 202410255, 202508284, 202507244, 202408015, 202505154, 202407305, 202411236, 2024112210, 202412105, 2025110512, 202501224, 202512154, 202407114, 202504294, 2025111910, 202407105, 202406266, 202501104, 202501275, 202503086, 2025040211, 2025111810, 2025041610, 2025110511, 202411054, 202408164, 202507104, 202408065, 202501286, 202503114, 202503214, 202412235, 202506024, 2024112111, 2024112010, 202505274, 202410304, 202411015, 202410225, 202408125, 202408205, 202409034, 202408165, 202510035, 202408155, 202408296, 202407154, 202407124, 202408064, 202406284, 202406205, 202601064, 2025122210, 2025111410, 202511066, 202411265, 202411225, 202411224, 202506104, 202408176, 202410294, 202512234, 202407015, 202407014, 202407125, 202504224, 202505014, 202411195, 202502064, 202411014, 202408094, 202411216, 202411214, 202504214, 202507094, 202406285, 202406244, 202502205, 202503205, 2024112610, 202412144, 202410235, 202411255, 202501246, 202408106, 202408224, 202407254, 202407024, 202504056, 202503245, 202501245, 202502075, 202501234, 202502114, 2024112011, 202411206, 202412135, 202406275, 202501024, 202411276, 202412124, 2024112211, 2024121210, 2025102310, 202512114, 202601055, 2025080710, 202506114, 202505284, 202505176, 202407314, 202408144, 202408134, 202410245, 202411194, 202411254, 2024121310, 202501025, 202501155, 202412114, 202408084, 202501086, 202502204, 202501034, 202412226, 202406254, 202509014, 2025100210, 202511076, 202503195, 202412164, 202407256, 202407116, 202411226, 202406286, 202407136, 202408194, 2025081110, 202411205, 202408146, 202411264, 202412234, 202411215, 202406226, 2025040710, 202501256, 202502055, 202410314, 202410284, 202408295, 202408145, 202408136, 202501154, 202502105, 202501236, 202411266, 202408124, 2024121311, 202503105, 2025040311, 202406255, 202407095, 202412125, 2024112510, 2025043010, 2024112110, 2024112511, 202408156, 202501226, 202408216, 202501085, 202407026, 2026010511, 2024071212, 202407126, 202410285, 202408166, 202406256, 202504174, 2024121211. *OUS added 06/10/2026 expansion: 202411204, 202511075, 202511244, 202509154, 202509104, 202509264, 202508084, 2025080611, 202507284, 202507254, 202507264, 202504174, 202506274, 2025040310, 202504244, 202505144, 202501085, 202501094, 202504164, 202502214, 2024112110, 202410245, 202410285, 202411044, 2024112011, 202412105, 202411266, 202510274, 202510184, 202406226, 202406216, 202407024, 202407136, 202408066, 2024071212, 202511064, 202511065, 202509274, 202508214, 202510254, 202506124, 202503204, 202504044, 202505064, 202503075, 202501244, 202501154, 202407026, 202408194, 202407116, 202511214, 2025071010, 202505164, 202410315, 202501166, 202512124, 202408304, 202410225, 202408135, 202511074, 202509124, 202510244, 2025100310, 202507144, 202505194, 2025041710, 202501084, 202406255, 202407126, 202408195, 202411214, 202408084, 202508204, 2025040410, 202411225, 202509114, 202503064, 202406256, 202407245, 202412124, 202511204, 202509254, 202510154, 202510034, 202504046, 2025040411, 202501235, 202501256, 202510035, 202512154, 202503065, 202407105, 202408144, 202506114, 202510204, 202512114, 202503245, 202501034, 202501224, 202411215, 202507244, 202509014, 202509244, 202508284, 202511086, 202511104, 202601064, 2024121210, 202408216, 202412234, 202502114, 202504056, 202411194, 2025043010, 202506134, 202507114, 202406245, 202408164, 2025080810, 202409034, 202508264, 202406214, 202408295, 202410294, 202504304, 202506164, 202506304, 202502105, 2024121311, 202410305, 202408146, 202504214, 202501164, 202601124, 202507234, 2025041610, 202501145, 202410284, 202408064, 202408136, 2… (truncated, 5687 characters total — see the official FDA record for the full value)
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 14, 2026

ConMed AirSeal 12mm Access Port and Palm Grip Obturator with Bladeless Optical Tip, 150mm Length. Catalog Number: iAS12-150LPI. 6 units per pack. Disposable Endoscopic Trocar and Cannula; Carbon Dioxide Insufflator for Laparoscopy.

Potential for overpressure alerts.

ALL 50 STATES
Full report

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

Recall #:
98854
Lot/product code:
Catalog Number: iAS12-150LPI. UDI-DI: 10845854052006. Lot Numbers: 202509234, 202506104, 202505074, 202503204, 202510094, 202510144, 202508194, 202506244, 202512054, 202512234, 202511224, 202504164, 202504074, 202407294, 202511214, 202410254, 202512184, 202412175, 202407115, 202411055, 202411284, 202408235, 202411274, 202502275. *OUS added 06/10/2026 expansion: 202510144, 202510094, 202506244, 202509234, 202504074, 202412175, 202408235, 202407294, 202508194, 202410254, 202408234, 202503204, 202506104, 202411055, 202505074, 202504164, 202512184, 202411274, 202511224, 202511214, 202601124, 202502275, 202411284, 202512054, 202407115. Manufactured from 14 June 2024 to 12 January 2026.
Recalling firm:
ConMed Corporation
View official FDA record (opens in a new tab)
Class IIILow risk
DrugRecalled May 14, 2026

Epinephrine Injection, USP, 1mg/mL, 1 mL single-dose vial, Rx only, Fresenius Kabi, Lake Zurich, IL 60047, NDC 63323-696-02 (vial), NDC 63323-696-25 (carton)

Failed Impurities/Degradations Specifications

ALL 50 STATES
Full report

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:
D-0581-2026
Lot/product code:
Batch # 6133313, 6133314, Exp Date: 06/2026; Batch # 6133315, Exp Date: 07/2026; Batch # 6133682, Exp Date: 09/2026; Batch # 6134812, 6134813, Exp Date: 04/2027.
Recalling firm:
Fresenius Kabi USA, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 14, 2026

Duloxetine DR Capsules, 30 mg, 30 count bottles, Rx, Relabeled by: Enovachem Pharmaceuticals, Torrance, CA 90501, NDC 76420-634-30, Marketed by: Ajanta Pharma USA Inc.

CGMP Deviations; presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the FDA acceptable intake limit.

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-0555-2026
Lot/product code:
Lot # 050725G-30 & 050725F-30, Exp Date: 06/30/2026
Recalling firm:
Asclemed USA Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide therapeutic benefit to those affected with advanced heart failure. In service, the LVAS assumes some or all of the workload of the left ventricle, thereby restoring the patient's systemic perfusion while palliating the underlying pathology. The LVAS features a Left Ventricular Assist Device (LVAD), a blood pump intended for long-term implantation in such patients, an extracorporeal Controller, plus all of the features, controls, attachments, interfaces, power sources, supporting equipment, labeling, and tools required to achieve the desired therapeutic benefit. Component: No

Due to 11 volt Backup Battery failures.

ALL 50 STATES
Full report

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

Recall #:
99023
Lot/product code:
Lot Code: Model Number: 106524US UDI/GTIN 05415067039323 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.
Recalling firm:
Thoratec LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Medtronic 1x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64001; Stimulator, electrical, implanted, for parkinsonian tremor

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

ALL 50 STATES
Full report

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

Recall #:
98913
Lot/product code:
GTIN 00643169090866, Lot Number VA368G3; GTIN 00643169090866, Lot Number VA36V7T; GTIN 00643169936584, Lot Number VA3347Y; GTIN 00643169936584, Lot Number VA33481; GTIN 00643169936584, Lot Number VA33M8V; GTIN 00643169936584, Lot Number VA33M92; GTIN 00643169936584, Lot Number VA33T31; GTIN 00643169936584, Lot Number VA33T33; GTIN 00643169936584, Lot Number VA35B5D; GTIN 00643169936584, Lot Number VA35B5E; GTIN 00643169936584, Lot Number VA35WSP; GTIN 00643169936584, Lot Number VA35WSU; GTIN 00763000963040, Lot Number VA35TTU; GTIN 00763000963040, Lot Number VA35TTV; GTIN 00763000963040, Lot Number VA368FZ; GTIN 00763000963040, Lot Number VA368G3; GTIN 00763000963040, Lot Number VA36V7T; GTIN 00763000963040, Lot Number VA36V8Q; GTIN 00763000968427, Lot Number 0231980220; GTIN 00763000968427, Lot Number 0231980221; GTIN 00763000968427, Lot Number 0231980222; GTIN 00763000968434, Lot Number 0231493884; GTIN 00763000968434, Lot Number 0231493885; GTIN 00763000968434, Lot Number 0231494066; GTIN 00763000968434, Lot Number 0231928923; GTIN 00763000968434, Lot Number 0231929188; GTIN 00763000968434, Lot Number 0231929189; GTIN 00763000968434, Lot Number 0231929192; GTIN 00763000968441, Lot Number 0231367316; GTIN 00763000968441, Lot Number 0231367317; GTIN 00763000968441, Lot Number 0231367319; GTIN 00763000968441, Lot Number 0231367320; GTIN 00763000968441, Lot Number 0231367321; GTIN 00763000968441, Lot Number 0231367322; GTIN 00763000968441, Lot Number 0231514399; GTIN 00763000968441, Lot Number 0231514400; GTIN 00763000968441, Lot Number 0231514401; GTIN 00763000968441, Lot Number 0231514402; GTIN 00763000968441, Lot Number 0231514403; GTIN 00763000968441, Lot Number 0231514404; GTIN 00763000968441, Lot Number 0231514405; GTIN 00763000968441, Lot Number 0231514406; GTIN 00763000968441, Lot Number 0231514407; GTIN 00763000968441, Lot Number 0231514408; GTIN 00763000968441, Lot Number 0231514409; GTIN 00763000968441, Lot Number 0231514410; GTIN 00763000968441, Lot Number 0231514411; GTIN 00763000968441, Lot Number 0231514412; GTIN 00763000968441, Lot Number 0231514413; GTIN 00763000968441, Lot Number 0231929193; GTIN 00763000968441, Lot Number 0231929194; GTIN 00763000968441, Lot Number 0231929195; GTIN 00763000968441, Lot Number 0231929196; GTIN 00763000968441, Lot Number 0231929197; GTIN 00763000968441, Lot Number 0231929198; GTIN 00763000968441, Lot Number 0231929199; GTIN 00763000968441, Lot Number 0231929200; GTIN 00763000968441, Lot Number 0231929201; GTIN 00763000968441, Lot Number 0232153351; GTIN 00763000968441, Lot Number 0232153352; GTIN 00763000968441, Lot Number 0232153353; GTIN 00763000968441, Lot Number 0232153354; GTIN 00763000968441, Lot Number 0232153355; GTIN 00763000968441, Lot Number 0232153360; GTIN 00763000968441, Lot Number 0232212159; GTIN 00763000968441, Lot Number 0232212160; GTIN 00763000968441, Lot Number 0232212161; GTIN 00763000968441, Lot Number 0232224165; GTIN 00763000968441, Lot Number 0232224206; GTIN 00763000968441, Lot Number 0232224207; GTIN 00763000968441, Lot Number 0232224208; GTIN 00763000968441, Lot Number 0232224209; GTIN 00763000968441, Lot Number 0232224211; GTIN 00763000968441, Lot Number 0232224212; GTIN 00763000968441, Lot Number 0232224213; GTIN 00763000968441, Lot Number 0232224214; GTIN 00763000968441, Lot Number 0232224215; GTIN 00763000968441, Lot Number 0232224216; GTIN 00763000968441, Lot Number 0232224217; GTIN 00763000968441, Lot Number 0232224218; GTIN 00763000968441, Lot Number 0232546510; GTIN 00763000968441, Lot Number 0232546511; GTIN 00763000968441, Lot Number 0232554256; GTIN 00763000968441, Lot Number 0232554257; GTIN 00763000968441, Lot Number 0232589003; GTIN 00763000968441, Lot Number 0232589646; GTIN 00763000968441, Lot Number 0232589647; GTIN 00763000968441, Lot Number 0232589648; GTIN 00763000968441, Lot Number 0232589649; GTIN 00763000968441, Lot Number 0232589651; GTIN 00763000968441, Lot Number 0232676531; GTIN 00763000968441, Lot Number 0232676532; GTIN 00763000968441, Lot Number 0232676533; GTIN 00763000968441, Lot Number 0232676534; GTIN 00763000968441, Lot Number 0232676535; GTIN 00763000968441, Lot Number 0232676536; GTIN 00763000968441, Lot Number 0232676537; GTIN 00763000968441, Lot Number 0232676539; GTIN 00763000968441, Lot Number 0232676540; GTIN 00763000968441, Lot Number 0232676541; GTIN 00763000968441, Lot Number 0232725690; GTIN 00763000968441, Lot Number 0232725694; GTIN 00763000968441, Lot Number 0232725695; GTIN 00763000968441, Lot Number 0232725696; GTIN 00763000968441, Lot Number 0232725699.
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Medtronic 2x4 Pocket Adaptor Kit for Deep Brain Stimulation, Model 64002; Stimulator, electrical, implanted, for parkinsonian tremor

A limited number of Pocket Adaptor Kits, Model 64001 and 64002, are labeled with incorrect Use-By-Dates.

ALL 50 STATES
Full report

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

Recall #:
98913
Lot/product code:
GTIN 00643169090866, Lot Number VA368G3; GTIN 00643169090866, Lot Number VA36V7T; GTIN 00643169936584, Lot Number VA3347Y; GTIN 00643169936584, Lot Number VA33481; GTIN 00643169936584, Lot Number VA33M8V; GTIN 00643169936584, Lot Number VA33M92; GTIN 00643169936584, Lot Number VA33T31; GTIN 00643169936584, Lot Number VA33T33; GTIN 00643169936584, Lot Number VA35B5D; GTIN 00643169936584, Lot Number VA35B5E; GTIN 00643169936584, Lot Number VA35WSP; GTIN 00643169936584, Lot Number VA35WSU; GTIN 00763000963040, Lot Number VA35TTU; GTIN 00763000963040, Lot Number VA35TTV; GTIN 00763000963040, Lot Number VA368FZ; GTIN 00763000963040, Lot Number VA368G3; GTIN 00763000963040, Lot Number VA36V7T; GTIN 00763000963040, Lot Number VA36V8Q; GTIN 00763000968427, Lot Number 0231980220; GTIN 00763000968427, Lot Number 0231980221; GTIN 00763000968427, Lot Number 0231980222; GTIN 00763000968434, Lot Number 0231493884; GTIN 00763000968434, Lot Number 0231493885; GTIN 00763000968434, Lot Number 0231494066; GTIN 00763000968434, Lot Number 0231928923; GTIN 00763000968434, Lot Number 0231929188; GTIN 00763000968434, Lot Number 0231929189; GTIN 00763000968434, Lot Number 0231929192; GTIN 00763000968441, Lot Number 0231367316; GTIN 00763000968441, Lot Number 0231367317.
Recalling firm:
Medtronic Neuromodulation
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A Product Description: The HeartMate 3" System Controller acts as the central power and communication hub for the HeartMate 3 LVAS. It passes power from the Power Module, the Mobile Power Unit, Lithium-Ion Batteries, or its own integrated emergency backup supply, down to the LVAD via the Driveline. The HeartMate 3 System Controller constantly monitors system performance through communication with the implanted LVAD and Controller internal measurements and alerts the user to any alarm conditions by activating membrane panel LEDs and integrated audio annunciators. Further information on alarm conditions as well as system status can be attained by the user from the front panel LCD on the System Controller. When connected to a HeartMate Touch" Communication System, the System Controller sends information regarding the System Controller and Pump Status once per second to provide additional information to the user. This link also allows the clinician to set new patient operating parameters (e.g. pump speed) and provides a link for downloading trend and/or event recorder data. Component: Yes, HeartMate 3 Left Ventricular System (LVAS) Kits

Due to 11 volt Backup Battery failures.

ALL 50 STATES
Full report

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

Recall #:
99023
Lot/product code:
Lot Code: Model Number:106531US UDI/GTIN: 05415067039446 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.
Recalling firm:
Thoratec LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model/Catalog Number: 106128 Software Version: N/A Product Description: The HeartMate 11 Volt Lithium Ion Standalone Backup Battery is a component of the HeartMate 3" System Controller and provides power to the System Controller. The HeartMate System Controller is an external device that manages the HeartMate Left Ventricular Assist System (LVAS), including alarms, system monitoring, and communication. It contains an internal 11V lithium-ion backup battery that provides at least 15 minutes of emergency power should the main system power source fail. The backup battery must be properly installed, charges automatically during normal use, and has a 36-month service life from date of manufacture. Component: Yes, HeartMate 3" System Controller

Due to 11 volt Backup Battery failures.

ALL 50 STATES
Full report

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

Recall #:
99023
Lot/product code:
Lot Code: Model Number: 106128 UDI/GTIN 05415067039880 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.
Recalling firm:
Thoratec LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodAllergenUndeclaredRecalled May 13, 2026

Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen

Not listed on the label Allergen (Soy)

Full report

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

Recall #:
H-0947-2026
Lot/product code:
Product Code: 40007; Lot Code: CH030426
Recalling firm:
Nutrisystem Inc
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684

Due to products are incorrectly flagged as expired due to the system's 24-hour usage limit, rendering the product unavailable for clinical procedures.

ALL 50 STATES
Full report

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

Recall #:
99176
Lot/product code:
ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100 ENDOFLIP 1 10884521808096 05391530810166 DL ENDOFLIP 1 10884521786684
Recalling firm:
Covidien, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Brand Name: HeartMate Product Name: HeartMate 3" System Controller Model/Catalog Number: 106531US Software Version: N/A Product Description: The HeartMate 3" System Controller acts as the central power and communication hub for the HeartMate 3 LVAS. It passes power from the Power Module, the Mobile Power Unit, Lithium-Ion Batteries, or its own integrated emergency backup supply, down to the LVAD via the Driveline. The HeartMate 3 System Controller constantly monitors system performance through communication with the implanted LVAD and Controller internal measurements and alerts the user to any alarm conditions by activating membrane panel LEDs and integrated audio annunciators. Further information on alarm conditions as well as system status can be attained by the user from the front panel LCD on the System Controller. When connected to a HeartMate Touch" Communication System, the System Controller sends information regarding the System Controller and Pump Status once per second to provide additional information to the user. This link also allows the clinician to set new patient operating parameters (e.g. pump speed) and provides a link for downloading trend and/or event recorder data. Component: Yes, HeartMate 3 Left Ventricular System (LVAS) Kits

Due to 11 volt Backup Battery failures.

ALL 50 STATES
Full report

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

Recall #:
99023
Lot/product code:
Lot Code: Model Number:106531US UDI/GTIN: 05415067039446 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.
Recalling firm:
Thoratec LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Brand Name: HeartMate Product Name: HM 11V Li-ion Backup Battery, ABT Model/Catalog Number: 106128 Software Version: N/A Product Description: The HeartMate 11 Volt Lithium Ion Standalone Backup Battery is a component of the HeartMate 3" System Controller and provides power to the System Controller. The HeartMate System Controller is an external device that manages the HeartMate Left Ventricular Assist System (LVAS), including alarms, system monitoring, and communication. It contains an internal 11V lithium-ion backup battery that provides at least 15 minutes of emergency power should the main system power source fail. The backup battery must be properly installed, charges automatically during normal use, and has a 36-month service life from date of manufacture. Component: Yes, HeartMate 3" System Controller

Due to 11 volt Backup Battery failures.

ALL 50 STATES
Full report

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

Recall #:
99023
Lot/product code:
Lot Code: Model Number: 106128 UDI/GTIN 05415067039880 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.
Recalling firm:
Thoratec LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

SafeOp Patient Interface, REF: AIX11240, part of SafeOp 3: Neural Informatix System

Intraoperative neuromonitoring device, due to a software issue, may experience loss or interruption of triggered electromyography (tEMG) functionality during use, displaying as system faults, loss of communication between the Patient Interface and Tablet, and prompts requiring system reboot; may result in increased operative time and surgical plan change.

ALL 50 STATES
Full report

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

Recall #:
98967
Lot/product code:
UDI-DI: 00190376517506. System Set ID/Patient Interface Serial Number: 2007716/ DG106225, 2005498/ DG106220, 2005490/ DG106230
Recalling firm:
Alphatec Spine, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 13, 2026

Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US Software Version: N/A Product Description: The HeartMate 3" Left Ventricular Assist System (LVAS) is a set of equipment and materials that together comprise a medical device designed to provide therapeutic benefit to those affected with advanced heart failure. In service, the LVAS assumes some or all of the workload of the left ventricle, thereby restoring the patient's systemic perfusion while palliating the underlying pathology. The LVAS features a Left Ventricular Assist Device (LVAD), a blood pump intended for long-term implantation in such patients, an extracorporeal Controller, plus all of the features, controls, attachments, interfaces, power sources, supporting equipment, labeling, and tools required to achieve the desired therapeutic benefit. Component: No

Due to 11 volt Backup Battery failures.

ALL 50 STATES
Full report

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

Recall #:
99023
Lot/product code:
Lot Code: Model Number: 106524US UDI/GTIN 05415067039323 Serial Numbers Distributed in US: See Attachment E for serial numbers distributed.
Recalling firm:
Thoratec LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodBacteria/virusRecalled May 13, 2026

Hellas Meze Golden Smoked Whole Herring

Un-eviscerated fish may be contaminated with clostridium botulinum

Full report

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

Recall #:
H-0899-2026
Lot/product code:
production date of 4/12/2025, best before 4/12/2026, L120425F54
Recalling firm:
Terra Medi LLC
View official FDA record (opens in a new tab)