Device evidence

device-recall:cfres:128901

VI DBL OFFST W/ LRG STPL, LT Nonsterile

Official recall number

Z-2219-2014

Evidence summary

Product code: LXH
Recall status: Terminated
Event initiated: July 23, 2014
Root cause: Device Design
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-2219-2014