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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:205205

LEFT SMALL-PCA MOD.REV.DUR.REV.INSERT Intended for knee replacement. Product Number: 6637-0-631

Official recall number

Z-0910-2024

Evidence summary

Product code
JWH
Recall status
Open, Classified
Event initiated
December 01, 2023
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0910-2024

Field note

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