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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:206815

ZPLP (Zimmer Periarticular Locking Plate System) Distal Lateral Fibular Plate, Left, 12 Holes, 184 MM, Sterile- Indicated for temporary internal fixation and stabilization of osteotomies and fractures Item Number: 47-2357-018-12

Official recall number

Z-1719-2024

Evidence summary

Product code
HWC
Recall status
Open, Classified
Event initiated
March 20, 2024
Root cause
Under Investigation by firm
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1719-2024

Field note

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