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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:128819

Cordis EMPIRA RX PTCA Dilatation Catheter

Official recall number

Z-2557-2014

Evidence summary

Product code
LOX
Recall status
Terminated
Event initiated
June 23, 2014
Root cause
Environmental control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2557-2014

Field note

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