Bard
8 federal recalls on file, showing the 7 from the last 12 months. We monitor every CPSC, FDA, USDA, and NHTSA notice for Bard and translate it into plain English — free weekly digest, optional same-day alerts.
- 2026-05-27FDA-DeviceClass IIC.R. Bard Silastic Foley Catheters recalled for surface stain
C.R. Bard has recalled certain Silastic Brand Foley Catheters (5cc and 30cc models) due to staining on the catheter surface. The affected catheters were distributed across the U.S. and Canada.
- 2026-02-25FDA-DeviceClass IIStop using affected Bard Broviac and Hickman catheters
Bard Peripheral Vascular is recalling multiple central venous catheter trays and kits because the outer packaging may be damaged, which could compromise the sterile barrier that protects the medical device. The recall affects several Broviac and Hickman catheter products with specific lot numbers manufactured between April 2028 and August 2030.
- 2025-12-17FDA-DeviceClass IICheck BD InLay Optima Ureteral Stent Kit labeling
C.R. Bard Inc. has recalled certain BD InLay Optima Ureteral Stent Kits (8 Fr. x 26 cm, REF 78826, Lot# NGJU4328) because the actual stent size may not match what the label says. This labeling error could lead to incorrect stent selection during medical procedures.
- 2025-12-17FDA-DeviceClass IICheck BD InLay Optima stent labeling
C.R. Bard Inc. is recalling a specific lot of BD InLay Optima Ureteral Stent Kits (6 Fr. x 30 cm, Ref 788630, Lot NGJU4327) because the actual stent size may not match what is printed on the product label. This discrepancy could affect proper stent selection and placement.
- 2025-12-17FDA-DeviceClass IICheck BD InLay Optima Ureteral Stent Kit labeling
BD InLay Optima Ureteral Stent Kits (4.7 Fr. x 26 cm, Lot NGJU4181) have a labeling error—the printed size on the package may not match the actual stent inside. This affects 4,350 units distributed across multiple U.S. states and internationally. No injuries have been reported.
- 2025-12-17FDA-DeviceClass IICheck C.R. Bard ureteral stent labeling
C.R. Bard Inc. is recalling certain InLay Optima ureteral stent kits (6 Fr. x 14 cm, REF 787614, Lot# NGJU4163) because the actual size of the stent may not match what is printed on the package label. This discrepancy could affect proper medical placement and treatment.
- 2025-12-17FDA-DeviceClass IIStop using Bard Safe-T-Centesis drainage trays
Bard Peripheral Vascular Inc. is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because the safety indicator on the catheter may show the wrong position—displaying "sharp" when the catheter is actually "blunt." This could lead medical staff to believe the catheter hasn't entered the body cavity when it actually has, potentially causing discomfort, treatment delays, or injury to organs or blood vessels.
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