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
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
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
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
AVID Medical Recalls Halyard MINI PLUS KIT SOUTH Over Transplant Risk
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.
AVID Medical
Devices are
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
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 Resection 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 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 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
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
Olympus Resection Sheath Recalled Due to 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 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 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
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
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 Resection Sheath Recalled Due to Breakage 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 Sheath Recalled Due to Breaking Tip Hazard
Olympus Corporation of the Americas recalled 2,626 units of its Resection Sheath on November 11, 2025. The ceramic tip of the sheath 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
Complaints of
Health & Personal Care
HIGH
FDA DEVICE
Olympus Resection Sheath Recalled Due to Breaking 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 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 Recalls 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
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 DEVICE
Olympus Resection Sheath Recalled Due to Ceramic Tip Breaking
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
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
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
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