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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:154669

RENOVATION, ROUNDED END, THIN OSTEOTOME BLADE, 12 MM, REF 71369412, STERILE R, QTY: (1)

Official recall number

Z-1919-2017

Evidence summary

Product code
KDG
Recall status
Terminated
Event initiated
March 30, 2017
Root cause
Error in labeling
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-1919-2017

Field note

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