FDAJuly 1, 2021device

ACCESS SARS-CoV-2 Antigen , REF: C68668, IVD, Rx only, UDI: (01) 15099590742713;

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

The hazard

SARS-CoV-2 Antigen Assay test may generate false positive results which could result in incorrect diagnosis .

What to do

FDA enforcement status: Terminated

Brands named

beckman coulterbeckman

UPCs

15099590742713

Recall history

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

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