Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:202524

LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF, Transcend LIF and Battalion LLIF,

Official recall number

Z-2475-2023

Evidence summary

Product code
HWJ
Recall status
Open, Classified
Event initiated
July 07, 2023
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2475-2023

Field note

Send feedback

We'll only use this to respond to your feedback.