Device evidence

device-recall:cfres:146712

LIFEPAK CR Plus and/or LIFEPAK EXPRESS are Automatic External Defibrillator(s) and are non-wearable. LIFEPAK CR Plus and LIFEPAK EXPRESS defibrillators are intended for use on patients in cardiac arrest.

Official recall number

Z-2100-2016

Evidence summary

Product code: MKJ
Recall status: Terminated
Event initiated: May 25, 2016
Root cause: Component change control
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-2100-2016