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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:139462

MediTrace Cadence Adult Zoll, Preconnect Defibrillation Electrode, Nonsterile Item Code:22770PC

Official recall number

Z-2546-2015

Evidence summary

Product code
DRO
Recall status
Terminated
Event initiated
August 19, 2015
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2546-2015

Field note

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