FDAMay 30, 2025device

Platelia Toxo IgM Catalog Number 26211 UDI Code: 03610520005552 The Platelia Toxo IgM assay is a semi-quantitative immunocapture enzyme immunoassay kit for the detection of IgM antibodies to Toxoplasma gondii in human serum, plasma or cord blood specimens.

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

The hazard

Due to a risk of false positive results that could lead to unnecessary medical treatment.

What to do

FDA enforcement status: Ongoing

Brands named

bio rad laboratoriesbiobio rad

UPCs

03610520005552

Recall history

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

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