Overview of recall records associated with Acon Biotech (Hangzhou) Co., Ltd., including dates, categories and classifications where available.
Classification mix: Class II: 1.
Non-EUA authorized, CE marked, SARS-CoV-2 antigen rapid test kits are being recalled from the U.S. market because use may lead to inaccurate test results, including false negative or false…
This page summarizes recall records in which the official source identifies Acon Biotech (Hangzhou) 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.
