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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:198117

WishBone Medical Smart Correction Dual Joint Express Struts, external skeleton fixation device Type Part Number XXS 10-702-080095-0 XS 10-702-095115-0 Short 10-702-115150-0 Medium 10-702-140200 Long 10-702-190300-0

Official recall number

Z-1102-2023

Evidence summary

Product code
KTT
Recall status
Open, Classified
Event initiated
January 04, 2023
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1102-2023