2,228 recalls tagged with “stop use 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 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.
Medline Industries recalled 4,853 surgical kits on January 7, 2026 due to potential sterility issues. Calibration problems with sterilization equipment could affect safety. Patients and providers must stop using these kits immediately.
Medline Industries recalled 240 units of convenience kits on January 7, 2026. Calibration issues with sterilization equipment may impact product safety. Patients and healthcare providers should stop using these devices immediately.
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.
Medline Industries recalled 4,525 surgical convenience kits on January 7, 2026, due to sterilization calibration issues. These problems could compromise sterility assurance levels, posing health risks. Healthcare providers and patients must stop using these products immediately.
Medline Industries recalled 23,238 convenience kits on January 7, 2026. The recall affects the BAPTIST FLOYD ENDO GI KIT and GI LAB OTHER ENDO KIT due to calibration issues that may compromise sterility. Patients and healthcare providers should stop using the 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 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 175 arthroscopy kits on January 7, 2026. Calibration issues with sterilization equipment may impact product sterility. Patients and healthcare providers should stop using the devices 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 30,958 convenience kits on January 7, 2026. Calibration issues with sterilization equipment may compromise product sterility. Healthcare providers and patients must stop using these products 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.
Ford is recalling 2025 Explorer SUVs, along with 2025 Transit and F-150 vehicles, due to defects in connecting rods and rod bearings. The issue can cause engine damage and failure. Owner notices were mailed August 15, 2025, and Ford recall number is 25S55. Dealers will inspect and replace the engine long block as needed.
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 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 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 2,724 OXIRIS SET dialyzers on January 6, 2026. The recall follows reports of potential dislodgement of the deaeration chamber from the Prismaflex Control Unit. Patients and healthcare providers must stop using the device immediately.