FDANovember 9, 2011device

ZYMUTEST HIA IgGAM. Model Number: RK040D. Qualitative screening assay for the detection of heparin-dependent antibodies (IgG, IgM and IgA isotypes by ELISA. 96 Tests.

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

The hazard

A voluntary recall is initiated for ZYMUTEST HIA lgGAM - Ref RK040D - Lot F1700415 and ZYMUTEST HIA MonoStrip lgGAM - Ref RK041D - Lot F1700416 because they may produce false positive results.

What to do

FDA enforcement status: Terminated

Brands named

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UPCs

03663537018770

Recall history

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

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