BrosMed Medical Co Hermes NC PTA Balloon Dilatation Catheter The balloon dilatation catheter recall — FDA Z-0963-2019
Incorrect (higher) Rated Burst Pressure information printed on label.
Overview of recall records associated with BrosMed Medical Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Incorrect (higher) Rated Burst Pressure information printed on label.
This page summarizes recall records in which the official source identifies BrosMed Medical Co., Ltd. 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.