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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:161798

ZYMUTEST HIA IgGAM. Model Number: RK040D. Qualitative screening assay for the detection of heparin-dependent antibodies (IgG, IgM and IgA isotypes by ELISA. 96 Tests.

Official recall number

Z-1062-2018

Evidence summary

Product code
LCO
Recall status
Terminated
Event initiated
November 09, 2011
Root cause
Other
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1062-2018

Field note

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