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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115914

ANSPACH***Arthroscopic Knotless Suture Anchor***Rx Only*** This device is intended to be used with Anspach Systems

Official recall number

Z-1915-2014

Evidence summary

Product code
MBI
Recall status
Terminated
Event initiated
November 28, 2012
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1915-2014