FDAFebruary 5, 2018device

ZYMUTEST HIA MonoStria qualitative screening assay intended for the global detection of heparin-dependent antibodies, whether the isotype is: IgG, IgM and IgA, in human plasma, by clinical laboratories. p IgGAM; REF Number: RK041D; UDI: 03663537046810

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

The hazard

Incorrect package insert indicating use of the kits with plasma, serum, and other biological fluids. The kits should only be used with plasma.

What to do

FDA enforcement status: Terminated

Brands named

hyphen biomedhyphen

UPCs

03663537046810

Recall history

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

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