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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:203962

Compress Device Segmental Anchor Plug, 16 MM-For Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. Item Number: 178406

Official recall number

Z-0373-2024

Evidence summary

Product code
KWA
Recall status
Open, Classified
Event initiated
October 09, 2023
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0373-2024

Field note

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