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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:166536

VENTANA ISH iView Blue Detection Kit, Catalog Number 05278511001, model 800-092 Immunohistochemistry (IHC) for in vitro diagnostic use.

Official recall number

Z-3008-2018

Evidence summary

Product code
PPM
Recall status
Terminated
Event initiated
August 02, 2018
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-3008-2018

Field note

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