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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:188960

Herniatome, 17G x 9cm, Cervical Type, Model Number 5091749

Official recall number

Z-0146-2022

Evidence summary

Product code
HRX
Recall status
Terminated
Event initiated
May 17, 2021
Root cause
Other
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0146-2022