Medical DeviceAug 8, 2018
QIAGEN EZ1 DSP Virus Kit (48), IVD, REF 62724 intended for in vitro diagnostic use recall — FDA Z-2596-2018
Underfilled reagent well that could lead to incorrect results
Class IIFDA: TerminatedQIAGEN
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 QIAGEN 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.