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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:199080

SMR TT Hybrid glenoid Std - Peg S, REF: 1379.59.210

Official recall number

Z-1317-2023

Evidence summary

Product code
MBF
Recall status
Open, Classified
Event initiated
February 21, 2023
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1317-2023

Field note

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