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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:176976

ORTHOFIX Catalogue Number: ref: 99-92504, PREFIX II ANKLE COMPLETE KIT STERILE, RX ONLY, UDI: (01)18033509855979

Official recall number

Z-0393-2020

Evidence summary

Product code
JDW
Recall status
Terminated
Event initiated
September 27, 2018
Root cause
Device Design
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0393-2020

Field note

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