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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:189748

ImplantDirect, REF 834713, Legacy 2 Implant 4.7mmD x 13mmL, 4.5mmD Platform,

Official recall number

Z-0198-2022

Evidence summary

Product code
DZE
Recall status
Open, Classified
Event initiated
September 23, 2021
Root cause
Packaging change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0198-2022