Overview of recall records associated with C.R. Bard, Inc., Urological Division, including dates, categories and classifications where available.
Classification mix: Class II: 2.
The 8 Fr. Bardex All-Silicone Foley Catheter with 3cc balloon had an incorrect inflation volume (10 ml instead of 5 ml) printed on the valve cap.
Incomplete seal on sterile packages of product.
This page summarizes recall records in which the official source identifies C.R. Bard, Inc., Urological Division as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
