FDAApril 21, 2020device

BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage: intended for the qualitative detection of total (IgG/IgM) antibodies to Treponema pallidum and the qualitative detection and/or titer determination of non-treponemal reagin anti...

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

The hazard

The increased level of RPR reactivity in the BioPlex 2200 Syphilis Total & RPR kit material number 12000650.

What to do

FDA enforcement status: Ongoing

Brands named

bio rad laboratoriesbiobio rad

UPCs

0361052065301203610520652770

Recall history

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

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