GS Biomark CoViPoint COVID test kit (MultiPLEX/Direct) Kit Item Numbers: BC-DK0200 recall — FDA Z-0324-2023
Distribution of COVID Test Kits without FDA Approval, Clearance or Authorization.
Overview of recall records associated with GS Biomark LLC, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Distribution of COVID Test Kits without FDA Approval, Clearance or Authorization.
This page summarizes recall records in which the official source identifies GS Biomark LLC 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.