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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:121961

BIOMET Spine, 5.5 TI 5.5x50mm Translation Screw Polaris 5.5 TI Spinal System. Rx Only. Non-Sterile. Intended for immobilization and stabilization as an adjunct to fusion as a pedicle screw fixation system

Official recall number

Z-0359-2014

Evidence summary

Product code
HWC
Recall status
Terminated
Event initiated
August 22, 2013
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0359-2014

Field note

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