1,716 recalls tagged with “cpsc regulated”.
Medline Industries recalled 39,315 surgical convenience kits on January 7, 2026. Calibration issues in sterilization equipment may compromise the sterility of these devices. Healthcare providers and patients should stop using these products immediately.
Olympus Corporation recalled 887 units of the Disposable Triple Lumen Sphincterotome on January 7, 2026. The devices may deform and lose performance if not properly thermoformed. The recall affects both US and international markets.
Medline Industries, LP recalled 154,427 Convenience Kits on January 7, 2026. The recall stems from calibration issues with sterilization equipment, potentially affecting sterility assurance. Patients and healthcare providers should stop using the affected products immediately.
CleverCut recalled 72,023 Single Use 3-Lumen Sphincterotome V devices on January 7, 2026. The devices may deform and lose performance due to a manufacturing issue. Healthcare providers and patients must stop using these instruments immediately.
Medline Industries recalled 15 units of its Triple Lumen Insertion Kits on January 7, 2026. The recall stems from calibration issues in sterilization equipment that may affect the product's sterility assurance level. Users should cease use immediately and follow manufacturer instructions.
Medline Industries recalled 9,051 surgical kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple model numbers and poses a high hazard risk. Patients and healthcare providers should stop using these products 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 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 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 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 recalled 27,320 convenience kits on January 7, 2026, due to calibration issues with sterilization equipment. These defects may compromise the sterility assurance level of the products. Healthcare providers and patients should stop using the affected kits immediately.
Medline Industries has recalled 779 units of its Convenience Kits due to calibration issues with sterilization equipment. The recall affects multiple model numbers including DYNJ56436A and DYNJ56436B. Consumers should stop using these products immediately and follow recall instructions.
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.
Carrot Top Kitchens recalled 12 units of White Truffle Hummus on January 6, 2026. The product contains undeclared sesame, posing a high risk to consumers with sesame allergies. The hummus was distributed in New York.
Carrot Top Kitchens recalled 12 units of Sundried Tomato and Caper Hummus on January 6, 2026. The product contains undeclared sesame, raising allergy concerns. Consumers should not eat this product.
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.
Encon Safety Products recalls AQ 120 GFEW Aquarion Preserved Cartridges sold nationwide through multiple retailers. The recall cites cGMP deviations in manufacturing. Stop using the product immediately and follow recall guidance from Encon Safety or your healthcare provider.
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.
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.
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.