Recall database

All Product Recalls

Browse 4,434 active product recalls and safety alerts. Use search and filters to narrow the list by product, brand, hazard level, or status.
Active recalls
4,434
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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
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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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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
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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
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