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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:126205

Zoll Medical X Series, PropaqMD, PropaqM Defibrillator/Pacemaker/Monitor With System Software Version 02.10.02.00 or Higher, automated external defibrillator.

Official recall number

Z-1311-2014

Evidence summary

Product code
MKJ
Recall status
Terminated
Event initiated
March 05, 2014
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1311-2014

Field note

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