Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:117214

Medi-Trace Cadence Adult Radiotransparent Defibrillation Electrode Product ID: 22550R. Intended for use in cardioversion, pacing, ECG monitoring, and defibrillation procedures.

Official recall number

Z-1184-2013

Evidence summary

Product code
DRO
Recall status
Terminated
Event initiated
April 08, 2013
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1184-2013

Field note

Send feedback

We'll only use this to respond to your feedback.