2,756 recalls tagged with “immediate action”.
Medline Industries recalled 32 units of Convenience Kits on January 7, 2026. Issues with sterilization equipment calibration may compromise device safety. Users should stop using the products immediately and follow recall instructions.
Medline Industries recalled 1,496 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects various models, potentially compromising sterility assurance levels. Patients and healthcare providers must stop using these devices 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 7,725 surgical kits on January 7, 2026, due to potential sterility issues. Calibration problems with sterilization equipment may compromise the sterility assurance level. Healthcare providers and patients should stop using these kits immediately.
Medline recalled 108 units of its Convenience Kits, model DYKMBNDL200A, due to calibration issues affecting sterility. The recall, issued on January 7, 2026, impacts products distributed worldwide. Healthcare providers and patients must stop using the kits 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 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 2,236 dental packs on January 7, 2026, due to calibration issues affecting sterilization. The recall impacts products distributed worldwide, raising safety concerns for healthcare providers. Consumers should stop using the recalled items immediately and follow manufacturer instructions.
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.
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, 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.
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.
Olympus Corporation of the Americas recalled 999 units of the Disposable Triple Lumen Sphincterotome on January 7, 2026. Devices may deform and lose performance due to improper thermoforming. Patients and healthcare providers should stop using the product immediately.
Medline Industries recalled 4,757 convenience kits on January 7, 2026, due to sterilization calibration issues. The recall affects multiple models, raising concerns about sterility assurance levels. Patients and healthcare providers should stop using these products 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 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.
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.
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.
Ford is recalling certain 2020-2025 Explorer and Aviator SUVs because the easy-entry second-row outer seat switch bezel may bind or stick, causing seats to unlatch, fold, or slide unexpectedly while driving. Dealers will inspect the second-row seat switch and replace the bezel around the switch as necessary, free of charge. Owner notification letters were mailed August 7, 2025; Ford can be reached
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.