Medical DeviceMar 28, 2018
Epigenomics Ag Epi proColon Plasma Quick Kit recall — FDA Z-1077-2018
The diagnostic test kit may produce invalid test runs which may delay test results.
Class IIFDA: TerminatedEpigenomics Ag
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Epigenomics Ag 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.