Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:160537

PROPONENT SR Pacemaker

Official recall number

Z-0373-2018

Evidence summary

Product code
LWP
Recall status
Open, Classified
Event initiated
December 07, 2017
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0373-2018

Field note

Send feedback

We'll only use this to respond to your feedback.