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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:184513

IceFORCE" 2.1 CX Cryoablation Needle

Official recall number

Z-0658-2021

Evidence summary

Product code
GEH
Recall status
Completed
Event initiated
November 18, 2020
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0658-2021

Field note

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