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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:181270

Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product Usage: is for use in the hospital by qualified medical personnel trained in the operation of the device and qualified by training in basic life support, advanced cardiac life support, or defibrillation

Official recall number

Z-2137-2020

Evidence summary

Product code
MKJ
Recall status
Terminated
Event initiated
April 21, 2020
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2137-2020

Field note

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