FDAJuly 15, 2020device

QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) - Product Usage: intended for the qualitative detection and differentiation of nucleic acid from multiple respiratory viral and bacterial organisms, including the SARS-CoV-2 virus, in nasopharyngeal swabs (NPS) eluted in un...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

There is an increased rate of potential false positive results for the Influenza A (no subtype) target, which may lead to 1) inappropriate antiviral use, 2) erroneous or delayed differential diagnosis and missing of an alternative diagnosis.

What to do

FDA enforcement status: Terminated

Brands named

qiagen sciencesqiagen

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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