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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:173613

SHERPA NX ACTIVE GUIDING CATHETER, 6F MP ST, .070", REF SA6MPST. for cardiovascular use

Official recall number

Z-2669-2019

Evidence summary

Product code
DQY
Recall status
Terminated
Event initiated
March 15, 2019
Root cause
Component design/selection
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2669-2019

Field note

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