FDAJuly 19, 2019device

ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use.

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

The hazard

Residual crystallization of the microplate and recurrent negative controls out of range.

What to do

FDA enforcement status: Terminated

Brands named

aniara diagnosticaaniara

Recall history

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

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