2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
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.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Multiple complaints were reported in which cracks formed in the hose of specific catheter mounts.
Defective Container - A defect in the side-seal which allows leakage of product.
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
Microbial Contamination of Sterile Products; out of limit results obtained for endotoxin testing.
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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.
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.
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.
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.
Safety and efficacy of dialysis acid concentrate cannot be assured
Diasol recalled 2,200 gallons of its 100425-10-DEX100 liquid concentrate for bicarbonate dialysis on November 5, 2025. The company cannot assure the safety and efficacy of the product. Patients and healthcare providers should stop using it immediately.
Product testing did not meet expected stability criteria.
Safety and efficacy of dialysis acid concentrate cannot be assured
Diasol recalled 4,400 gallons of its 100230-10-DEX100 dialysis acid concentrate on November 5, 2025. The company cannot assure the safety and efficacy of this product. Healthcare providers and patients must stop using the concentrate immediately.
Diasol recalled 4,400 gallons of its dialysis liquid concentrate on November 5, 2025. The recall follows concerns that the safety and efficacy of the product cannot be assured. Healthcare providers and patients should stop using the product immediately.
Safety and efficacy of dialysis acid concentrate cannot be assured
Defective container - seal not adhering to bottles
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