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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115542

Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The HeartStart XL+ is intended for use in a hospital setting by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced life support or defibrillation

Official recall number

Z-0871-2013

Evidence summary

Product code
MKJ
Recall status
Terminated
Event initiated
January 28, 2013
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0871-2013