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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:187198

10G DIRECT SINGLE BONE ACCESS KIT. For use in Orthopedic / spinal procedures.

Official recall number

Z-1743-2021

Evidence summary

Product code
NDN
Recall status
Terminated
Event initiated
March 25, 2021
Root cause
Vendor change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1743-2021

Field note

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