Device evidence

device-recall:cfres:160475

ACCOLADE MRI DR Pacemaker

Official recall number

Z-0358-2018

Evidence summary

Product code: LWP
Recall status: Open, Classified
Event initiated: December 07, 2017
Root cause: Device Design
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0358-2018