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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:203330

stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502

Official recall number

Z-0113-2024

Evidence summary

Product code
PHX
Recall status
Open, Classified
Event initiated
September 15, 2023
Root cause
Process change control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0113-2024

Field note

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