These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,247 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Medline Industries recalled 7,494 neuro shunt kits on January 7, 2026, due to sterilization calibration issues. These problems could compromise the sterility assurance level of the products. Patients and healthcare providers should stop using the affected devices immediately.
Medline Industries, LP recalled 551 units of convenience kits on January 7, 2026. Calibration issues in sterilization equipment may affect product sterility. Healthcare providers and patients must stop using the kits immediately.
Medline Industries recalled 291 units of burn care kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Users should stop using the affected products immediately.
Medline Industries recalled 753 tracheostomy kits on January 7, 2026, due to calibration issues in sterilization equipment. The defect may compromise the sterility assurance level of the devices. Users should stop using these products immediately and follow the recall instructions.
Medline Industries recalled 808 lithotomy packs on January 7, 2026, due to calibration issues in sterilization equipment. These problems may compromise the sterility assurance level of the products. Healthcare providers and patients must stop using these devices immediately.
Medline Industries recalled 1,070 ADMIT KITS due to calibration issues affecting sterilization. The recall, effective January 7, 2026, has been classified as Class II. Healthcare providers must stop using these kits immediately to ensure patient safety.
Medline Industries, LP recalled 684 medical convenience kits on January 7, 2026. The recall affects the LVAD Driveline Tray and the KIT Surg Onc Insert Cent. Venou due to calibration issues impacting sterility. Health providers and patients should stop using these products immediately.
Medline recalled 553 units of its Convenience Kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Healthcare providers and patients must stop using the affected devices immediately.
Medline Industries recalled 2,740 surgical kits on January 7, 2026. Calibration issues with sterilization equipment jeopardize the sterility assurance level of the products. Healthcare providers and patients must stop using these devices immediately.
Ford Motor Company recalled certain 2025 Explorer vehicles due to engine defects. The recall affects vehicles with potentially faulty connecting rods that could lead to engine failure. Owners received notification letters on August 15, 2025, and should contact Ford for repairs.
Ford Motor Company recalled certain 2025 F-250 SD vehicles due to a defect in the brake system. The brake booster pushrod retaining spring may not have been installed, risking sudden brake failure. Owners should not drive these vehicles until repairs are completed.
Ford Motor Company recalled certain 2020-2025 Explorer vehicles due to a potential seat malfunction. The issue involves the second-row outer seat switch, which may bind or stick, causing the seats to unlatch unexpectedly. This recall affects multiple units and was announced on January 6, 2026.
cGMP deviations.
VANTIVE US HEALTHCARE recalled 115,112 units of the PRISMAFLEX HF1000 SET on January 6, 2026. The recall stems from a potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.
VANTIVE US Healthcare recalled 230,596 units of the PRIMSAFLEX M100 Set on January 6, 2026. The recall follows a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.
VANTIVE US HEALTHCARE recalled 87,436 Prismaflex ST100 Dialyzers on January 6, 2026. The recall follows reports of potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately.
VANTIVE US Healthcare recalled 137,576 Prismaflex M150 Sets on January 6, 2026. The recall addresses a risk of dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
VANTIVE US HEALTHCARE recalled 13,760 Prismaflex TPE2000 Sets on January 6, 2026, due to a potential dislodgement hazard. The recall affects the deaeration chamber of the Prismaflex Control Unit. Healthcare providers and patients must stop using the device immediately.
HerbsForever recalled 45 units of its Gastro Care Ayurvedic Herbal Supplement on January 6, 2026. The recall follows the discovery of a potential undeclared allergen, wheat, which poses a serious risk to consumers with wheat allergies. Affected products were sold online nationwide.
Herbs Forever recalled 45 units of Hingwastika Churna on January 6, 2026. The product may contain undeclared wheat, posing a health risk to consumers with wheat allergies. Customers should stop using the product immediately and contact the company for a refund or replacement.