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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:173544

SHERPA NX ACTIVE GUIDING CATHETER, 6F RCB, .070", REF SA6RCB. for cardiovascular use

Official recall number

Z-2645-2019

Evidence summary

Product code
DQY
Recall status
Terminated
Event initiated
March 15, 2019
Root cause
Component design/selection
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-2645-2019

Field note

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