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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:137035

PRI Femoral Impactor Block for knee prosthesis surgery. Orthopedic Manual Surgical Instrument

Official recall number

Z-1696-2015

Evidence summary

Product code
LXH
Recall status
Terminated
Event initiated
April 30, 2015
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1696-2015

Field note

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