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Consumer Product Recalls

127,244 recalls from the U.S. Consumer Product Safety Commission, newest first.

November 26, 2025Medical DevicesFDA
Medtronic Perfusion Systems recalls MC3 VitalFlow Console, REF 58100; Blood pump of ecmo
Hazard: As of August 6, 2025, Medtronic has received eleven reports of VitalFlow Consoles displaying an E70 error code during normal operation. When this occurs, the touch screen may become temporarily unresponsive and go blank for up to two minutes before recovering to full functionality. Importantly, the console continues to maintain set pump speed and function throughout.
November 26, 2025Medical DevicesFDA
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone) Model/Catalog Number: 106017, HeartMate II¿
Hazard: Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.
November 26, 2025Medical DevicesFDA
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate II¿ LVAS Implant Kit Model/Catalog Number: 106015, HeartMate II¿ LVAS Ki
Hazard: Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.
November 26, 2025Medical DevicesFDA
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone) Model/Catalog Number: 106531US, HeartMate 3 Co
Hazard: Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.
November 26, 2025Medical DevicesFDA
Thoratec LLC recalls Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US, He
Hazard: Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.
November 26, 2025Medical DevicesFDA
Becton Dickinson & Company recalls BD Luer Tip Caps; Catalog Number(s) or Model Number(s): 308341;
Hazard: BD has confirmed through internal testing that certain device trays failed routine biocompatibility testing.
November 26, 2025Medical DevicesFDA
ELEKTA SOLUTIONS AB recalls MOSAIQ Oncology Information System Software Builds 3.1.3, 3.2.1, 3.2.2 & 3.2.3.0 Software Version and UDI Codes: 3
Hazard: When appending a care plan that contains one or more wave medication orders, the occurrence and frequency of the appended orders may not match the intended schedule.
November 26, 2025Medical DevicesFDA
TMJ Solutions Inc recalls TMJ Bilateral Implant REF: CHG020 Sterile EO, Rx Only
Hazard: Patient-fitted temporomandibular joint implant contained discrepancy in screw hole position.
November 26, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris infusion Pump Module 8100, REF: 8100; KIT, BEZEL ASSY 8100BD, REF: 49000437; KIT ASSY ONE PIECE BEZEL 8100,
Hazard: If infusion pump is dropped or severely jarred this may damage the pump module bezel assembly, which can cause under-infusion, over-infusion, unregulated flow, or pump module failure to calibrate; so dropped/jarred pumps should be removed from use, tested, and inspected by qualified service personnel prior to reuse; tip sheet, cleaning and disinfecting procedure and reference guide updated.
November 26, 2025Food & BeverageFDA
BULK & ORGANIC LLC recalls Bulk and Organic Organic Moringa Powder, 44.1lbs bag
Hazard: Possible Salmonella Richmond
November 26, 2025Food & BeverageFDA
Haitai, Inc. recalls Cinnamon Powder; 8oz clear plastic container. Distributed by Haitai Inc. UPC: 0 20914 81415 9
Hazard: Elevated levels of lead in Cinnamon powder.
November 26, 2025Food & BeverageFDA
New Hoque and Sons, Inc. recalls Dry Ghoinnya Fish
Hazard: Un-eviscerated fish may be contaminated with Clostridia botulinum.
November 26, 2025Food & BeverageFDA
Plenus Group Inc. recalls Rockport Lobser Bisque; packed in 2x8lb pouches and in 4x4b pouches
Hazard: Products contain undeclared shrimp (crustacean shellfish)
November 26, 2025Food & BeverageFDA
Peterson Company Inc recalls Item# 29608 Farmhouse White, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz.
Hazard: Item #29608 Farmhouse White is recalled due to E. coli O103:H2.
November 26, 2025Food & BeverageFDA
Peterson Company Inc recalls Item# 28855 Whatcom Blue, Twin Sisters Creamery brand, product is packed in Cryovac and each package weighs 5oz-6oz. The
Hazard: Item #28855 Whatcom Blue is recalled due to E. coli O103:H2
November 26, 2025Food & BeverageFDA
Twin Sisters Creamery, LLC recalls Twin Sisters Creamery Mustard Seed cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. I
Hazard: Raw milk Mustard Seed cheese is recalled due to E. coli O103:H2 and E. coli O74:H25.
November 26, 2025Food & BeverageFDA
Twin Sisters Creamery, LLC recalls Twin Sisters Creamery Peppercorn cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ing
Hazard: Raw milk Peppercorn cheese is recalled due to E.coli O26:H11
November 26, 2025Food & BeverageFDA
Twin Sisters Creamery, LLC recalls Twin Sisters Creamery Farmhouse Cheese, 3lb. round cheese wheel, made with raw milk and aged at minimum of 60 days. Ingr
Hazard: Raw milk Farmhouse cheeses are recalled due to E. coli O103:H2 and E. coli O74:H25.
November 26, 2025Food & BeverageFDA
Twin Sisters Creamery, LLC recalls Twin Sisters Creamery Whatcom Blue cheese, 2.5lb. round cheese wheel, made with raw milk and aged at minimum of 60 days.
Hazard: Raw milk Whatcom Blue cheese is recalled due to E. coli O103:H2.
November 26, 2025Food & BeverageFDA
Publix Super Markets, Inc. recalls Publix Rich & Creamy Vanilla Ice Cream
Hazard: Undeclared Eggs
November 26, 2025DrugsFDA
Otsuka ICU Medical LLC recalls POTASSIUM CHLORIDE Inj., 10 mEq total in 100 mL Flexible Container, Highly concentrated 100 mEq/L, Rx Only, ICU Medical,
Hazard: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
November 26, 2025DrugsFDA
Otsuka ICU Medical LLC recalls POTASSIUM CHLORIDE Inj., 20 mEq total in 50 mL Flexible Container, Highly concentrated 400 mEq/L, Rx Only, ICU Medical,
Hazard: Labeling: Label Error on Declared Strength-The overwrap label may incorrectly identify the product as POTASSIUM CHLORIDE Inj. 10 mEq instead of POTASSIUM CHLORIDE Inj. 20 mEq
November 26, 2025DrugsFDA
Park Avenue Compounding recalls Fentanyl citrate, 2 mcg / ml / Ropivacaine, 0.2% in NS 150 mL, CII, 150 mL bag, Rx Only, Park Avenue Compounding, 3662
Hazard: CGMP Deviations: Revised interpretation of Acceptable Quality Level (AQL) results.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls UltraSure Anti-Perspirant & Deodorant, Aluminum Sesquichlorohydrate 15%, 118 mL (4 fl. oz.), DermaRite Industries LLC, 7
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls San-E-Foam, Alcohol 67%, 1000 mL (34 fl. oz.) per cartridge, DermaRite Industries LLC, 7777 West Side Avenue, North Berg
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls Renew Skin Repair Cream, Dimethicone 1.5%, packaged in a) 5g tube (NDC 61924-405-05), b) 4 oz tube (NDC 61924-405-04), a
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls Renew PeriProtect, Zinc Oxide 12%, Dimethicone 1%, 113g (4 oz.) per tube, DermaRite Industries LLC, 7777 West Side Avenu
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls PeriGuard Ointment, Petrolatum 49.9%, packaged in a) 5g (NDC 61924-205-05), b) 3.5oz (NDC 61924-205-04), and c) 7oz (NDC
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls PeriGiene, Health Care Antiseptic, Chloroxylenol 0.5%, 222mL (7.5 fl. oz.) bottle, DermaRite Industries LLC, 7777 West S
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.
November 26, 2025DrugsFDA
DermaRite Industries, LLC recalls McKesson Skin Protectant, Lanolin USP, packaged in a) 5g (NDC 68599-6202-1), and b) 4oz NDC 68599-6203-4 tube, Distribu
Hazard: CGMP Deviation; manufactured at the same facility where other products and lots were found to be contaminated.