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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-2346-2019 - ZYMUTEST HIA MonoStrip, IgG ELISA kit, Model No. RK041A, for in vitro diagnostic use. 2 08/22/2019 FEI # 3005017664
Aniara Diagnostica LLC
Z-2347-2019 - ZYMUTEST HIA MonoStrip, IgGAM ELISA kit, Model No. RK041D, for in vitro diagnostic use. 2 08/22/2019 FEI # 3005017664
Aniara Diagnostica LLC
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