Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:197302

Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cutting and shaping bone including the spine and cranium

Official recall number

Z-0921-2023

Evidence summary

Product code
HBC
Recall status
Open, Classified
Event initiated
December 07, 2022
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0921-2023