Hyphen BioMed recalls

5 recalls on record · latest: February 5, 2018

Official U.S. recall history for Hyphen BioMed, compiled from official government records.

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Hyphen BioMed recalls ZYMUTEST HIA MonoStria qualitative screening assay intended for the global detection of heparin-dependent antibodies, w…

February 5, 2018 · Medical device recalls Moderate risk Incorrect package insert indicating use of the kits with plasma, serum, and oth…

Hyphen BioMed recalls ZYMUTEST HIA IgGAM; REF Number: RK040D; UDI: 03663537018770 a qualitative screening assay intended for the global detec…

February 5, 2018 · Medical device recalls Moderate risk Incorrect package insert indicating use of the kits with plasma, serum, and oth…

Hyphen BioMed recalls ZYMUTEST HIA MonoStrip IgG; REF Number: RK041A; UDI: 03663537046803 a qualitative assay intended for the detection of h…

February 5, 2018 · Medical device recalls Moderate risk Incorrect package insert indicating use of the kits with plasma, serum, and oth…

Hyphen BioMed recalls ZYMUTEST HIA IgGAM. Model Number: RK040D. Qualitative screening assay for the detection of heparin-dependent antibodies…

November 9, 2011 · Medical device recalls Moderate risk A voluntary recall is initiated for ZYMUTEST HIA lgGAM - Ref RK040D - Lot F1700…

Hyphen BioMed recalls ZYMUTEST HIA MonoStrip IgGAM. Model Number: RK041D. Qualitative screening assay for the detection of heparin-dependent…

November 9, 2011 · Medical device recalls Moderate risk A voluntary recall is initiated for ZYMUTEST HIA lgGAM - Ref RK040D - Lot F1700…