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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:137092

ANSPACH -4MM Coarse Diamond Ball, 22MM Shaft Exposure; REF S-4DC-22-G1 Cutting shaping bone including spine and cranium.

Official recall number

Z-2307-2015

Evidence summary

Product code
HBE
Recall status
Terminated
Event initiated
April 13, 2015
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2307-2015

Field note

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