Overview of recall records associated with FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)CO., LTD, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The "DVOT brand" rapid test kits have not obtained the necessary authorization to be sold in the United States.
This page summarizes recall records in which the official source identifies FENG CHUN YUAN MEDICAL EQUIPMENT (SHENZHEN)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.
