2,153 recalls tagged with “stop use immediately”.
Medline Industries recalled 7,575 PPE kits on January 7, 2026, due to calibration problems affecting sterilization. The recall involves model number DYK1011945P, distributed worldwide. Users should stop using the affected kits immediately and follow manufacturer instructions.
Medline Industries, LP recalled over 70 million surgical gowns on January 7, 2026, due to sterilization calibration issues. These issues may compromise the sterility assurance level of the gowns, posing a potential health risk. Healthcare providers and patients should stop using these gowns immediately and follow the recall instructions.
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.
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.
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.
Olympus Corporation of the Americas recalled 1,025 units of its Single Use 3-Lumen Sphincterotome V on January 7, 2026. The devices may deform due to inadequate thermoforming, posing a high hazard level. Patients and healthcare providers must stop using the devices immediately and follow recall 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 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.
Medline Industries recalled 448 units of its BASIC NERVE BLOCK TRAY W/LINEN on January 7, 2026. The recall stems from calibration issues with sterilization equipment that may affect the product's sterility assurance level. Healthcare providers should stop using the device immediately and follow the provided instructions.
Medline Industries recalled 150 units of its Convenience Kits on January 7, 2026. Calibration issues with sterilization equipment may affect the sterility assurance level of the products. Patients and healthcare providers must stop using the devices 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 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 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 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