2,153 recalls tagged with “stop use immediately”.
Olympus Corporation of the Americas recalled 1,676 units of Resection Sheath Model No. A22042A on November 11, 2025. Complaints indicated the ceramic tip of the sheath could break during use, posing a hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 91 units of the Inner Sheath Model No. A4741 on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled the Resection Sheath Model A2666T on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard for patients. Healthcare providers and patients should stop using the device immediately.
Olympus Corporation of the Americas recalled 118 units of its 28 Fr. resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a risk of injury. Healthcare providers and patients must stop using the device immediately.
AVID Medical recalled 132 units of its Organ Recovery Kit on November 11, 2025. The devices are not suitable for organ transplant, posing a high risk to patients. Healthcare providers and patients should stop using the device immediately and follow recall instructions.
Olympus Corporation of the Americas recalled 437 units of the Inner Sheath, Model No. WA22017A, on November 11, 2025. The recall follows complaints of the ceramic tip breaking during use, posing a significant risk to patients. Healthcare providers and patients should cease use immediately and follow the manufacturer’s instructions.
Olympus Corporation recalled 899 units of the Resection Sheath Model No. A42011A on November 11, 2025. Complaints indicate that the ceramic tip may break during use, posing a high risk to patients. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled the Inner Sheath Model No. A2660 on November 11, 2025. Complaints of the ceramic tip breaking prompted the recall of nine units distributed nationwide. Patients and healthcare providers must stop using the device immediately.
Olympus Corporation of the Americas recalled 7,426 units of the A22040T resection sheath on November 11, 2025. The recall follows reports of the ceramic tip breaking, posing a high hazard to patients. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation recalled the Resection Sheath, Model No. A2666, on November 11, 2025, following complaints of the ceramic tip breaking. The recall affects one unit distributed nationwide in the U.S. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled 6,949 units of its Resection Inner Sheath on November 11, 2025, after reports of the ceramic tip breaking. This device, used in urologic applications, poses a high hazard risk. Healthcare providers and patients should stop using the device immediately.
Olympus Corporation of the Americas recalled the Inner Sheath 21 Fr., Model No. A2660T, on November 11, 2025. The recall follows reports of the ceramic tip breaking during use. Patients and healthcare providers should stop using the device immediately.
AVID Medical recalled 380 units of the Halyard MINI PLUS KIT SOUTH on November 11, 2025. The devices are unsuitable for organ transplant procedures, posing potential health risks. Healthcare providers and patients must stop using the device immediately.
Olympus Corporation of the Americas recalled 3,484 units of the Resection Sheath Model No. A22041A on November 11, 2025. Reports indicate the ceramic tip of the device may break during use, posing a serious hazard to patients. Healthcare providers and patients must stop using the device immediately and follow recall instructions.
Olympus Corporation recalled 29 units of its Resection Sheath on November 11, 2025. The recall affects model numbers A22014A and A22014T due to complaints of the ceramic tip breaking. The company advises immediate cessation of use and adherence to recall instructions.
AVID Medical recalled 52 units of the ORGAN RECOVERY OR PACK, Kit Code: LLOF1000-17, on November 11, 2025. The devices are unsuitable for organ transplant procedures, presenting a serious health risk. Healthcare providers must stop using the device immediately and follow recall instructions.
Waldemar Link GmbH & Co. KG recalled 18 units of the Endo Model Knee Fusion Nail SK on November 10, 2025. The device features a preassembled locking screw incorrectly inserted, posing a high risk of failure. Affected units were distributed in Alabama, Georgia, and Texas.
Draeger recalled 191,470 units of the ErgoStar CM 45 airway connector on November 10, 2025. Users reported cracks in the hose of specific catheter mounts, posing a high risk to patients. The recall affects healthcare facilities worldwide, including multiple U.S. states.
Beckman Coulter recalled 76,098 units of COULTER DxH Diluent on November 10, 2025. The recall affects specific lots contributing to elevated platelet background counts in analyzers. Healthcare providers and patients must stop using this product immediately.
Draeger recalled 14,420 units of its ErgoStar CM 40 airway connector on November 10, 2025, due to cracks forming in the hose. The recall affects multiple states in the U.S. and several countries worldwide.