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Consumer Product Recalls

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

January 7, 2026DrugsFDA
Novo Nordisk Inc. recalls Wegovy (semaglutide) Injection, 1 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880 Ba
Hazard: Presence of Particulate Matter: Hair was found in a prefilled syringe
January 7, 2026DrugsFDA
Novo Nordisk Inc. recalls Wegovy (semaglutide) Injection, 0.5 mg/0.5 mL, 4 Single-Dose Prefilled Pens, Manufactured by: Novo Nordisk A/S, DK-2880
Hazard: Presence of Particulate Matter: Hair was found in a prefilled syringe
January 7, 2026DrugsFDA
CareFusion 213, LLC recalls BD ChloraPrep" Triple Swabsticks (Chlorhexidine gluconate (CHG), 2% w/v and Isopropyl alcohol (IPA), 70% v/v), 5.25 mL A
Hazard: Lack of Assurance of Sterlity
January 7, 2026TiresNHTSA
Aptany Tires recall
Hazard: Sidewall separation can cause tire failure, increasing the risk of a crash.
January 6, 2026VehiclesNHTSA
Blue Bird 2026 Equipment Adaptive/Mobility recall
Hazard: An unsecured wheelchair can move during transit, increasing the risk of injury.
January 5, 2026VehiclesNHTSA
Rivian 2022–2025 Suspension recall
Hazard: The toe link joint may separate, increasing the risk of a crash.
January 5, 2026VehiclesNHTSA
Blue Bird 2022–2024 Electrical System recall
Hazard: A loss of brake assist, drive power, steering assist, or instrument panel displays can increase the risk of a crash.
January 5, 2026Vehicle EquipmentNHTSA
LS2 Equipment recall
Hazard: A helmet that does not provide adequate protection increases the risk of injury during a crash.
January 2, 2026VehiclesNHTSA
Volvo 2025 Electrical System recall
Hazard: A high-voltage battery that overheats increases the risk of a fire.
December 31, 2025Medical DevicesFDA
Beckman Coulter Ireland, Inc. recalls BECKMAN COULTER BICARBONATE REF: OSR6137 OSR6237 OSR6637 OSR6x37 Bicarbonate is a system reagent for the quantitat
Hazard: Bicarbonate reagent may generate falsely high Bicarbonate results due to interference with Lactate Dehydrogenase (LDH) in the test sample.
December 31, 2025Medical DevicesFDA
Medtronic Neuromodulation recalls Restore Clinician Programmer Application (CP App), Model A71100 used with the following programmers: CT900A PROG CT90
Hazard: Software issue where a Device Reset message displayed on the app was unable to be cleared. In rare cases, this resulted in an inability to resume therapy, and the patient experienced a recurrence of underlying pain symptoms. Resolution would require surgical replacement of the INS.
December 31, 2025Medical DevicesFDA
Cook Incorporated recalls R¿sch-Uchida Transjugular Liver Access Sets, Reference Part Numbers: RUPS-100; The R¿sch-Uchida Transjugular Liver Ac
Hazard: Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
December 31, 2025Medical DevicesFDA
Cook Incorporated recalls Ring Transjugular Intrahepatic Access Sets, Reference Part Numbers: 1) RTPS-100; 2) RTPS-100-10.0; The Ring Trans
Hazard: Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
December 31, 2025Medical DevicesFDA
Cook Incorporated recalls Flexor Check-Flo Introducers and Sets, Reference Part Numbers: 1) KCFW-9.0-18/38-45-RB-ANL0-HC; 2) KCFW-9.0-18/38-4
Hazard: Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.
December 31, 2025Medical DevicesFDA
Diasol, Inc recalls Brand Name: Diasol Product Name: 100425-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0C
Hazard: Safety and efficacy of dialysis acid concentrate cannot be assured
December 31, 2025Medical DevicesFDA
Diasol, Inc recalls Brand Name: Diasol Product Name: 100325-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0C
Hazard: Safety and efficacy of dialysis acid concentrate cannot be assured
December 31, 2025Medical DevicesFDA
Diasol, Inc recalls Brand Name: Diasol Product Name: 100230-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0C
Hazard: Safety and efficacy of dialysis acid concentrate cannot be assured
December 31, 2025Medical DevicesFDA
Diasol, Inc recalls Brand Name: Diasol Product Name: 100220-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0C
Hazard: Safety and efficacy of dialysis acid concentrate cannot be assured
December 31, 2025Medical DevicesFDA
Diasol, Inc recalls Brand Name: Diasol Product Name: 100125-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0C
Hazard: Safety and efficacy of dialysis acid concentrate cannot be assured
December 31, 2025Medical DevicesFDA
Diasol, Inc recalls Brand Name: Diasol Product Name: 100225-10-DEX100, Liquid Concentrate for Bicarbonate Dialysis Non Pyrogenic, 2K, 3.0C
Hazard: Safety and efficacy of dialysis acid concentrate cannot be assured
December 31, 2025Medical DevicesFDA
Microbiologics Inc recalls LYFO DISK, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325L
Hazard: Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
December 31, 2025Medical DevicesFDA
Microbiologics Inc recalls KWIK-STIK 6-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325K
Hazard: Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
December 31, 2025Medical DevicesFDA
Microbiologics Inc recalls KWIK-STIK 2-Pack, Campylobacter jejuni subsp. jejuni derived from ATCC 29428, Catalog Number 0325P
Hazard: Affected units may fail to recover the target microorganism Campylobacter jejuni subsp. jejuni derived from ATCC 29428.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.
December 31, 2025Medical DevicesFDA
Zimmer, Inc. recalls Brand Name: Affixus Antegrade Femoral Nailing System Product Name: Affixus Antegrade Femoral Nails Model/Catalog Number:
Hazard: Affected implants may have undersized distal diameter along length of the shaft, which could lead to implant fatigue fracture. Potential health risk if implant fatigue fracture occurs include adverse local tissue reaction, pain or ache, non-union or malunion, or tissue damage necessitating surgical intervention.