MESA BIOTECH Accula SARS-CoV-2 Test, REF: COV4100 recall — FDA Z-1009-2022
SARS-CoV-2 Test has an increased potential for false positive results, which may lead to a delay in correct diagnosis and treatment.
Overview of recall records associated with MESA BIOTECH, Inc., including dates, categories and classifications where available.
Classification mix: Class I: 1.
SARS-CoV-2 Test has an increased potential for false positive results, which may lead to a delay in correct diagnosis and treatment.
This page summarizes recall records in which the official source identifies MESA BIOTECH, Inc. 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.