FDAAugust 12, 2019device

ZEUS ELISA Parvovirus B19 IgM Test System, UDI 00845533001755 - Product Usage: intended for the qualitative detection of IgM class antibodies to human Parvovirus B19 in human serum including women of childbearing age where there is a suspicion of exposure to human Parvovirus B19.

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

The hazard

FDA inspection identified that due to increased positivity (false positives) on the Parvovirus B19 ELISA Test System, the firm assigned a new Correction Factor and new lot number to the remainder of the affected lot, and distributed the reworked product to the customer.

What to do

FDA enforcement status: Terminated

Brands named

zeus scientificzeus

UPCs

00845533001755

Recall history

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

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