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All product recalls associated with Bard Access Systems, Inc.
Total Recalls
249
Past Year
18
Class I (Serious)
5
Most Recent
Nov 2025
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
Packaging for some gastrostomy tubes was labeled with incorrect balloon inflation data. An underinflated balloon may cause misplacement, slippage or premature removal of the tube. If an underinflated balloon allows the tube to be placed, or slip into, the stomal tract and not the stomach, there is a risk of infusion of fluids into the peritoneum. This carries the risk of infection.
The canes were made of unacceptable materials and could break
Device sterility may be compromised as evidenced by a loss of package integrity.