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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:191975

HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8

Official recall number

Z-0960-2022

Evidence summary

Product code
ITX
Recall status
Terminated
Event initiated
February 11, 2022
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0960-2022