6 recalls found for C.R. Bard. Check if any of your products are affected.
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 Inc recalled 116 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall stems from a labeling discrepancy where the actual stent size may not match the product label. This recall affects distribution in multiple U.S. states and several countries worldwide.
C.R. Bard recalled 116 units of its InLay Optima Ureteral Stent Kit on November 6, 2025. A labeling discrepancy may cause the actual size of the stent to differ from what is indicated on the label. The recall affects distribution across the U.S. and several countries worldwide.
C.R. Bard recalled 4,350 units of the InLay Optima Ureteral Stent Kit on November 6, 2025. The recall was initiated due to a labeling discrepancy where the actual size of the stent may not match its label. This affects distribution across the U.S. and several countries worldwide.
4,300 SureStep Foley Tray System Bardex I.C. Complete Care catheter tray units are recalled nationwide by C.R. Bard. The trays may contain incorrect inserts, creating a risk of infection or an allergic reaction. Healthcare providers and patients should stop using the device and follow Bard’s recall instructions.
C.R. Bard Inc. recalls 4,300 SureStep Foley Tray System Lubri-Sil I.C. Complete Care infection control Foley catheter trays nationwide in the United States. The trays may contain incorrect inserts that misrepresent material composition. The mismatch could trigger infections or allergic reactions. Health care providers should stop use and follow recall instructions immediately.