Category hub
High activity category
This category has a significant number of recalls. Check it regularly if you own products in this area.
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.
Complaints of the ceramic tip of the resection sheath breaking have been received.
Devices are not suitable for organ transplant.
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.
Devices are not suitable for organ transplant.
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.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
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.
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 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.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
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.
Defective Container - A defect in the side-seal which allows leakage of product.
The recall involves Neaude BR0221SL001 adult portable bed rails sold on Amazon. It poses a serious entrapment and asphyxiation risk. Consumers should stop using the recalled rails and start the refund process with Neaude now.
C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual stent size to differ from the labeled size. Healthcare providers and patients should stop using the device immediately.
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
CareFusion 303 recalled 189 BD Alaris Pump Modules on November 6, 2025. The recall affects connectivity to hospital networks due to daylight savings time adjustments. Users should stop using the device immediately and follow manufacturer instructions.
Bard Peripheral Vascular recalled 1,240 Safe-T-Centesis Catheter Drainage Trays due to safety indicator defects. The recall affects products distributed nationwide since November 6, 2025. The defect may cause serious injuries during use in medical procedures.