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Consumer Product Recalls
127,277 recalls from the U.S. Consumer Product Safety Commission, newest first.
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: G5S-80C; Software Version: NA Product Descrip
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5S-01C, (2) G5S-02C, (3) G5S-10C, (4) G5S-
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-01C, (2) G5A-02C, (3) G5A-05C, (4) G5A-
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80C, (2) G5A-80C-TSO. Software Version
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-80A, (2) G5A-80A-TSO. Software Version
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
ZOLL Medical Corporation recalls Brand Name: ZOLL Product Name: Powerheart G5 AED Model/Catalog Number: (1) G5A-00A, (2) G5A-01A, (3) G5A-02A, (4) G5A-
Hazard: The potential for devices to fail their self-test as a result of prolonged exposure to extreme environments (temperature and/or humidity).
March 19, 2025Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls COR Disposable Kit, 8 mm w/ Perpendicularity. Cartilage Transplant System.
Hazard: Device is missing the pin in the graft loader component.
March 19, 2025Medical DevicesFDA
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls COR Disposable Kit, 8 mm. Cartilage Transplant System.
Hazard: Device is missing the pin in the graft loader component.
March 19, 2025Medical DevicesFDA
TruAbutment Inc. recalls Brand Name: TruScan Body, REF CN38-SB Product Name: TruScan Body compatible with CONELOG 3.8 Model/Catalog Number: CN
Hazard: Retroactive: Due to defect and quality issues dental scanner may not scan properly/accurately
March 19, 2025Medical DevicesFDA
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH951R, Negus Tonsil Forceps HVY-CVD 190MM; (2) REF BH952R
Hazard: The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
March 19, 2025Medical DevicesFDA
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF FB458R, Glover ATR.CLAMP CVD 215MM; (2) REF FB459R, Glover
Hazard: The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
March 19, 2025Medical DevicesFDA
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH198R, Fuchsig Artery Forceps CVD.190MM; (2) REF BH304R,
Hazard: The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
March 19, 2025Medical DevicesFDA
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BH100R, Carrel Artery Forceps 85MM; (2) REF BH104R, Hartmann
Hazard: The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
March 19, 2025Medical DevicesFDA
Aesculap Inc recalls Numerous models of nonsterile hemostatic forceps: (1) REF BJ500R, Phaneuf Hysterectomy Forceps STR 210MM; (2) REF BJ
Hazard: The forceps have been used in ways not covered by the design resulting in breakage of the clamps.
March 19, 2025Medical DevicesFDA
CardioFocus, Inc. recalls CardiFocus Heartlight X3 Catheter- Intended in the treatment of atrial fibrillation. It is introduced percutaneously in
Hazard: Damage to the sterile barrier pouch of catheter, which could potentially compromise its sterility.
March 19, 2025Medical DevicesFDA
Medtronic Perfusion Systems recalls Aortic Root Cannula: 1. DLP Aortic Root Cannula A. CANNULA 11012 AR FLOWGUARD 12GA, model no 11012 B. CANNULA 11014
Hazard: Unexpected loose material in the male luer used in the aortic root cannula has been identified. Potential harms when identified prior to use - procedure delay. Potential harm if not identified and used - stroke (reversible and irreversible).
March 19, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Care Coordination Engine (CCE) Infusion Adapter, Safety Management Software
Hazard: Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
March 19, 2025Medical DevicesFDA
CareFusion 303, Inc. recalls BD Alaris Systems Manager , REF 9601 Infusion Safety Management Software
Hazard: Software issue that may result in outdated automated programming request(APR) being sent to the progressive care unit (PCU).
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution CT ES, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution CT, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution Apex Select, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution Apex Plus, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution Apex Expert, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution Apex Elite, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
GE Medical Systems, LLC recalls GE Healthcare Revolution Apex, System, X-ray, Tomography, Computed
Hazard: GE HealthCare has become aware of a potential issue on certain Revolution CT and Revolution Apex series CT systems (please see affected product details and the Appendix) that can result in coolant fluid (glycol) leaking onto the floor near the base of the gantry. The fluid is visible as it has a blue color. It is not corrosive and is not at a harmful temperature. However, there is a potential for injury if the fluid is not noticed and a person slips and/or falls.
March 19, 2025Medical DevicesFDA
Smiths Medical ASD, Inc. recalls Portex Endotracheal Tube, Item Codes 100/105/025 100/105/030 100/105/035 100/111/020 100/111/025 100/111/030 100/111/035
Hazard: Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, underdose, or cardiopulmonary collapse.
March 19, 2025Food & BeverageFDA
Trinidad Benham Corp recalls Black Beans, Dried, net wt. 16 OZ (1 LB) 454g, packaged in plastic bag. Packaged in the U.S. UPC 0 70552 70412 1. DISTRI
Hazard: Elevated levels of MBC (carbendazim) thiophanate-methyl.
March 19, 2025Food & BeverageFDA
LITTLE LEAF FARMS LLC recalls Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Hazard: Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.
March 19, 2025Food & BeverageFDA
Mauna Loa Macadamia Nut Company, LLC recalls Mauna Loa Milk Chocolate Covered Macadamias product is a snack product and packaged in plastic 1oz pouch. Each carton co
Hazard: Undeclared almonds
March 19, 2025Food & BeverageFDA
ZB Importing LLC recalls Ulker Dankek Roll Cake Banana, item 9620, 8.3oz foil pack, 8 per case, UPC 8690504067986
Hazard: Wheat not listed in Contains statement