medical Class II Updated 2019-08-28

Aniara Diagnostica LLC recalls ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, f

Recalled Product

ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, for in vitro diagnostic use.


Hazard / Issue

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

Issued by

FDA

Affected States: NC, NH, NY, OH
Lot/Code Info: F1701571
View official government recall

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