Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:112530

Armada 35/ Armada 35 LL PTA Catheters. The device is intended for dilatation of lesions in the vasculature.

Official recall number

Z-2450-2012

Evidence summary

Product code
LIT
Recall status
Terminated
Event initiated
August 20, 2012
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2450-2012