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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:147445

Calix T PEEK Lumbar System, TLIF Rasp

Official recall number

Z-0126-2017

Evidence summary

Product code
MAX
Recall status
Terminated
Event initiated
May 17, 2016
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0126-2017

Field note

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