Medical Device Recalls
-
1 to 3 of 3 Results
Related Medical Device Recalls |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Z-1742-2018 - ZYMUTEST HIA MonoStrip IgG; REF Number: RK041A; UDI: 03663537046803 a qualitative assay intended for the detection of heparin-dependent antibodies of the IgG isotype, in human plasma, by clinical labo... | 2 | 05/08/2018 | Hyphen BioMed |
Z-1744-2018 - ZYMUTEST HIA IgGAM; REF Number: RK040D; UDI: 03663537018770 a qualitative screening assay intended for the global detection of heparin- dependent antibodies, whether the isotype is: IgG, IgM and IgA, ... | 2 | 05/08/2018 | Hyphen BioMed |
Z-1743-2018 - 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 laboratorie... | 2 | 05/08/2018 | Hyphen BioMed |
-