American Catheter / Cholangiogram Catheter 9100 Series recall — FDA Z-2191-2015
Catheters were not sealed before sterilization. and was not detected through subsequent acceptance activities, product release and distribution.
Overview of recall records associated with American Catheter Corp, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Catheters were not sealed before sterilization. and was not detected through subsequent acceptance activities, product release and distribution.
This page summarizes recall records in which the official source identifies American Catheter Corp 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.