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All product recalls associated with C. R.Bard, Inc./BardElectrophysiology Division.
Total Recalls
82
Past Year
11
Class I (Serious)
0
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.
Failure to insert the guidewire through the introducer needle.
Gastrostomy device anti-reflux valve may allow leakage from the stomach.
Metal guidewires used in Hemodialysis Catheters may have been reverse loaded within the dispenser. Potential exists for the stiff end of the guidewire to be inserted into the patient instead of the flexible end.