Device evidence

device-recall:cfres:159792

LIFEPAK 20e DEFIBRILLATOR/MONITOR, 3201273 Product Usage: The LIFEPAK 20e defibrillator/monitor is intended for use in the hospital, physician s office, and clinic setting by personnel who are authorized by a physician/medical director. It is intended for use on a crash cart as well as for portable emergency response throughout a hospital.

Official recall number

Z-0294-2018

Evidence summary

Product code: MKJ
Recall status: Terminated
Event initiated: December 04, 2017
Root cause: Other
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-0294-2018