Device evidence

device-recall:cfres:116918

Presource PBDS, Shoulder Arthroscopy, Kit, Circulator

Official recall number

Z-1200-2013

Evidence summary

Product code: OFP
Recall status: Terminated
Event initiated: March 26, 2013
Root cause: Packaging process control
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1200-2013