Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115465

NEUROPATH 6Fx100 GUIDING CATH HH Product Code: GHH61000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

Official recall number

Z-0864-2013

Evidence summary

Product code
DQY
Recall status
Terminated
Event initiated
January 11, 2013
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0864-2013