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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115451

NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for use in the coronary, peripheral, and neurovasculature for intravascular introduction of interventional/diagnostic devices

Official recall number

Z-0850-2013

Evidence summary

Product code
DQY
Recall status
Terminated
Event initiated
January 11, 2013
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0850-2013