Bard
8 federal recalls on file. 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
Due to stain present on the surface of affected foley catheters.
- 2026-02-25FDA-DeviceClass IIStop using affected Bard Broviac and Hickman catheters
Due to damage to outer tray that can potentially compromise the sterile barrier
- 2025-12-17FDA-DeviceClass IICheck BD InLay Optima Ureteral Stent Kit labeling
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- 2025-12-17FDA-DeviceClass IICheck BD InLay Optima stent labeling
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- 2025-12-17FDA-DeviceClass IICheck BD InLay Optima Ureteral Stent Kit labeling
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- 2025-12-17FDA-DeviceClass IICheck C.R. Bard ureteral stent labeling
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
- 2025-12-17FDA-DeviceClass IIStop using Bard Safe-T-Centesis drainage trays
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that erroneously show catheter in sharp position when catheter is in blunt position, which may lead users to believe device is not yet in pleural or peritoneal space when it is, may cause discomfort, delay to treatment, injury to internal organs or vessels.
- 2021-10-13FDA-DeviceClass IIStop using Bard TIN3015 aspiration needles
Potential for needle protector to become fully dislodge exposing infusion needle which could result in needle stick.
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