Wuxi Medical lnstrument Factory Co ViaMed Alcohol Prep Pads, For External Use Only, 70% recall — FDA D-0247-2025
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
Overview of recall records associated with Wuxi Medical lnstrument Factory Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.
This page summarizes recall records in which the official source identifies Wuxi Medical lnstrument Factory 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.