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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:179536

Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017

Official recall number

Z-1271-2020

Evidence summary

Product code
MKJ
Recall status
Terminated
Event initiated
September 10, 2019
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1271-2020

Field note

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