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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
September 25, 2025VehiclesNHTSA
IC BUS 2026 Visibility recall
Hazard: An inoperative wiper can reduce the driver's ability to see out of the windshield, increasing the risk of a crash.
September 25, 2025VehiclesNHTSA
Chevrolet 2024 Forward Collision Avoidance recall
Hazard: A vehicle that fails to make sufficient sound may result in pedestrians being unaware of an approaching vehicle, increasing the risk of injury.
September 25, 2025Vehicle EquipmentNHTSA
Cognito Motorsports Suspension recall
Hazard: An upper control arm that disengages can cause a loss of steering, increasing the risk of a crash.
September 25, 2025Vehicle EquipmentNHTSA
Mopar Structure recall
Hazard: Detached trim pieces can create a road hazard for other vehicles, increasing the risk of a crash.
September 25, 2025Car SeatsNHTSA
Evenflo Child Seat recall
Hazard: Pieces of foam can present a choking hazard to a child, increasing the risk of injury.

September 25, 2025OtherCPSC
Persilux Brand Zebra Blinds Recalled Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violates Federal Rule for Window Coverings; Sold on Amazon
Hazard: The recalled blinds have long operating cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The blinds violate the federal rule for window coverings and present a substantial product hazard. In addition, the blinds also violate labeling requirements for window coverings.

September 25, 2025OtherCPSC
Autoez Brand Bamboo Shades Recalled Due to Strangulation and Entanglement Hazards and Risk of Serious Injury or Death; Violates Federal Rule for Window Coverings; Sold on Walmart.com
Hazard: The recalled shades have long operating cords and accessible inner cords that can cause death or serious injury to children, due to strangulation and entanglement hazards. The shades violate the federal rule for window coverings and present a substantial product hazard. In addition, the shades also violate labeling requirements for window coverings.

September 25, 2025OtherCPSC
Mad Rabbit Recalls "RELIEVE" Lidocaine Numbing Cream Due to Risk of Serious Injury or Death from Poisoning to Young Children; Violates Mandatory Standard for Child-Resistant Packaging
Hazard: The numbing cream contains lidocaine, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The numbing cream's packaging is not child-resistant, posing a risk of serious injury or death from poisoning, if the contents are swallowed by young children.

September 25, 2025Children's ProductsCPSC
AMTRADING Recalls Hoovy Cooling Gel Insert Pads for Car Seats and Strollers Due to Burn Hazard
Hazard: The cooling gel pads can become hot if left in the sun or a hot car, posing a burn hazard to young children.

September 25, 2025AppliancesCPSC
Sunbeam Products Recalls More than One Million Oster French Door Countertop Ovens Due to Burn Hazard
Hazard: The oven's doors can unexpectedly close, posing a burn hazard to consumers.
September 24, 2025Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray, REF: A942216
Hazard: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
September 24, 2025Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System Lubri-Sil I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303414A
Hazard: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
September 24, 2025Medical DevicesFDA
C.R. Bard Inc recalls SureStep Foley Tray System Bardex I.C. Complete Care Infection Control Foley Catheter Tray, REF: A303316A
Hazard: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when it's natural rubber latex, or 2)Natural rubber latex with infection control coating, when it's silicone hydrogel with antimicrobial coating, or 3)Natural latex with infection control, when it's silicone hydrogel coated without antimicrobial coating, which may cause infection and/or local and/or systemic allergic reaction
September 24, 2025Medical DevicesFDA
Maquet Cardiovascular, LLC recalls Heartstring III Proximal Seal System, 4.3 MM. Intravascular anastomosis occluder.
Hazard: Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.
September 24, 2025Medical DevicesFDA
Maquet Cardiovascular, LLC recalls Heartstring III Proximal Seal System, 3.8 MM. Intravascular anastomosis occluder.
Hazard: Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.
September 24, 2025Medical DevicesFDA
Maquet Cardiovascular, LLC recalls Heartstring III Proximal Seal System. Intravascular anastomosis occluder.
Hazard: Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.
September 24, 2025Medical DevicesFDA
Abbott Point Of Care Inc. recalls i-STAT EG6+ cartridge. List Number: 03P77-25.
Hazard: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
September 24, 2025Medical DevicesFDA
Abbott Point Of Care Inc. recalls i-STAT EG7+ cartridge. List Number: 03P76-25.
Hazard: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
September 24, 2025Medical DevicesFDA
Abbott Point Of Care Inc. recalls i-STAT CG8+ cartridge. List Number: 03P88-25. 510(k) numbers: K894914, K940918, K223710, K230275, K230285, K230300
Hazard: Lack of a 510(k) premarket clearance for the i-STAT CG8+, EG7+ and EG6+ cartridges to reflect updated sample type for potassium and ionized calcium and measurement ranges for pH and PO2.
September 24, 2025Medical DevicesFDA
Abbott Point Of Care Inc. recalls i-STAT CG4+ cartridge (white). List Number: 03P85-25.
Hazard: Lack of a 510(k) premarket clearance for the i-STAT CG4+ cartridge to reflect updated sample type for lactate and measurement ranges for pH and PO2.
September 24, 2025Medical DevicesFDA
Folsom Metal Products, Inc. recalls Frontier Devices, REF: 301.916S1, 16 mm Distraction Pin, 10 single packs , Rx Only, Sterile
Hazard: Labeling includes shelf life that has not been validated.
September 24, 2025Medical DevicesFDA
Folsom Metal Products, Inc. recalls Frontier Devices, REF: 301.914S2, 14 mm Distraction Pin, 10 double packs , Rx Only, Sterile
Hazard: Labeling includes shelf life that has not been validated.
September 24, 2025Medical DevicesFDA
Folsom Metal Products, Inc. recalls Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 10 single packs , Rx Only, Sterile
Hazard: Labeling includes shelf life that has not been validated.
September 24, 2025Medical DevicesFDA
Folsom Metal Products, Inc. recalls Frontier Devices, REF: 301.914S1, 14 mm Distraction Pin, 5 single packs , Rx Only, Sterile
Hazard: Labeling includes shelf life that has not been validated.
September 24, 2025Medical DevicesFDA
Folsom Metal Products, Inc. recalls Frontier Devices, REF: 301.912S2, 12 mm Distraction Pin, 10 double packs , Rx Only, Sterile
Hazard: Labeling includes shelf life that has not been validated.
September 24, 2025Medical DevicesFDA
Folsom Metal Products, Inc. recalls Frontier Devices, REF: 301.912S1, 12 mm Distraction Pin, 10 single packs , Rx Only, Sterile
Hazard: Labeling includes shelf life that has not been validated.
September 24, 2025Medical DevicesFDA
Beckman Coulter Inc. recalls UniCel DxH 600 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF:B23858
Hazard: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.
September 24, 2025Medical DevicesFDA
Beckman Coulter Inc. recalls UniCel DxH 800 COULTER Cellular Analysis System, configured with the Led HGB Photometer REFs:B24802, 629029, B63322
Hazard: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.
September 24, 2025Medical DevicesFDA
Beckman Coulter Inc. recalls UniCel DxH 690T COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C34520
Hazard: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.
September 24, 2025Medical DevicesFDA
Beckman Coulter Inc. recalls UniCel DxH 900 COULTER Cellular Analysis System, configured with the Led HGB Photometer REF: C11478
Hazard: Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.