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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:122062

***REF IMRI-MOTOR***iMRI Handpiece. Use with iMRI System Only***Rx Only***Manufacturer: The Anspach Effort, Inc. Intended for cutting and shaping bone.

Official recall number

Z-0657-2014

Evidence summary

Product code
HBB
Recall status
Terminated
Event initiated
April 25, 2013
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0657-2014