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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:213359

Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual language)

Official recall number

Z-1694-2025

Evidence summary

Product code
MKJ
Recall status
Open, Classified
Event initiated
March 18, 2025
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1694-2025

Field note

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