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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:190571

DYNANAIL MINI, Endcap +6mm, REF 2600-05-006, Rx Only, Sterile

Official recall number

Z-0453-2022

Evidence summary

Product code
HWC
Recall status
Open, Classified
Event initiated
November 17, 2021
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0453-2022

Field note

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