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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:180592

X12+ and patient cable for the X12+ Telemeter with the following device name: PAT CBL 10WIRE LEADFORM AHA SNAP, PAT CBL 10WIRE LEADFORM IEC SNAP, PAT CBL 10WIRE LEADFORM XL AHA SNAP, PAT CBL 10WIRE LEADFORM XL IEC SNAP, PAT CBL 4WIRE AHA SNAP HC.

Official recall number

Z-1814-2020

Evidence summary

Product code
DPS
Recall status
Terminated
Event initiated
March 18, 2020
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1814-2020

Field note

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