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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:212354

A.L.P.S. mvX- MEDIAL TIBIA PLATE 6H RT-Medial Tibia Plate, 6-Hole, Right Model/Catalog Number: 770715062 Intended for Fixation of fractures of the distal tibia

Official recall number

Z-1220-2025

Evidence summary

Product code
HRS
Recall status
Open, Classified
Event initiated
January 21, 2025
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1220-2025

Field note

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