2,056 recalls tagged with “cpsc regulated”.
Medline Industries recalled 117,907 surgical convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects numerous models, including spinal and knee procedure kits. Patients and healthcare providers should stop using these devices immediately.
Medline Industries recalled 4,415 surgical kits on January 7, 2026, due to sterilization calibration issues. These issues could compromise the sterility assurance level of the products. Healthcare providers and patients must stop using the kits immediately.
Medline Industries recalled 193,157 surgical packs on January 7, 2026, due to sterility assurance issues. The recall affects two model numbers: DYNJP1050UG and DYNJP8401. Healthcare providers and patients must stop using these products immediately.
Medline recalled 5,346 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple model numbers, potentially compromising their sterility assurance. Healthcare providers and patients must stop using the products immediately.
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 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 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.
Ford Motor Company recalls 2025 F-250 SD and other SD models for a brake pedal pushrod retaining spring that may not be installed. The defect can cause a sudden loss of brake function and a crash risk. Owners should not drive the vehicle until repaired. Ford will inspect and repair the brake pedal assembly free of charge; letters were mailed June 20, 2025.
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.
VANTIVE US Healthcare recalled 93,576 Prismaflex HF1000 Sets on January 6, 2026. The recall addresses a potential dislodgement of the deaeration chamber from the control unit. Healthcare providers and patients must stop using the device immediately and follow provided instructions.
Karison Foods & Snacks, Inc. recalled 2,760 units of NO SUGAR ADDED BESAN LADDOO on January 6, 2026. The product contains undeclared milk, posing a serious risk to those with dairy allergies. Consumers should stop using the product immediately and seek a refund.