immediate action Recalls

2,756 recalls tagged with “immediate action”.

Health & Personal Care
HIGH
FDA DEVICE

C.R. Bard Ureteral Stent Kit Recalled Due to Labeling Discrepancy

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.

C.R. Bard
Labeling discrepancy;
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