Health & Personal Care
HIGH
FDA DEVICE
Olympus Inner Sheath Recalled Due to Ceramic Tip Breakage Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
immediate action Recalls
2,756 recalls tagged with “immediate action”.
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breaking Ceramic Tip
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Inner Sheath Recalled Due to Breakage Risk
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.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Inner Sheath Recalled Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Inner Sheath Recalled Due to Ceramic Tip Risk
Olympus recalled its Inner Sheath, Model No. A2642, on November 11, 2025, due to safety complaints. Users reported the ceramic tip of the resection sheath breaking during use. This recall affects urological applications and poses a high risk to patients.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalls Inner Sheath Due to Breaking Ceramic Tip Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Sheath Recalled Over Risk of Ceramic Tip Breakage
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Ceramic Tip Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Inner Sheath Recalled Over Breaking Ceramic Tip Hazard
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Inner Sheath Recalled Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Recalled Endoscopic Sheath Due to Breakage Risk
Complaints of the ceramic tip of the resection sheath breaking have been received.
Olympus Corporation of the Americas
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
AVID Medical Recalls Organ Recovery Kit Due to Unsuitability
Devices are not suitable for organ transplant.
AVID Medical
Devices are
Health & Personal Care
HIGH
FDA DEVICE
Medline Recalls DEXLOCK Achilles Repair Implant Kits Due to Surgical Risk
There have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill guide may prolong the surgical procedure.
Medline Industries, LP
There have
Health & Personal Care
HIGH
FDA DRUG
Dr. Reddy's Labs Recalls Varenicline Tablets Over Potency Issues
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.
VARENICLINE TARTRATE
Sub potent
Health & Personal Care
HIGH
FDA DEVICE
Draeger Recalls Airway Connector Due to Cracking Hazard
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Draeger
Multiple complaints
Health & Personal Care
HIGH
FDA DEVICE
Draeger Recalls Airway Connector Over Cracking Hazard
Draeger recalled 118,850 airway connectors on November 10, 2025, due to cracking hazards. This recall affects multiple countries, including the United States and Australia. The device poses a serious risk to mechanically ventilated patients.
Draeger
Multiple complaints
Health & Personal Care
HIGH
FDA DEVICE
Waldemar Link Recalls Knee Fusion Nail Due to Assembly Error
The device has been delivered with a preassembled locking screw that had been inserted from the wrong side into the male taper of the femoral component.
Waldemar Link GmbH & Co. KG
The device
Health & Personal Care
HIGH
FDA DEVICE
Draeger Recalls Airway Connector Over Cracking Hazard
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.
Draeger
Multiple complaints
Health & Personal Care
HIGH
FDA DEVICE
Draeger Recalls Airway Connector Due to Cracks in Hose
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Draeger
Multiple complaints
Health & Personal Care
HIGH
FDA DEVICE
Beckman Coulter Recalls Diluent Due to Elevated Platelet Counts
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.
Beckman Coulter
Due to
Tag Statistics
Total Recalls
2,756