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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:176254

Stryker Neurovascular, Merci 9F, 80cm, Balloon Guide Catheter, REF 90077, CE 0459, UPN Product No. 90077, UDI #: (01)00815742000771

Official recall number

Z-0065-2020

Evidence summary

Product code
DQY
Recall status
Terminated
Event initiated
November 13, 2018
Root cause
Labeling False and Misleading
Source snapshot
d51b4b87fdeb9ccf809d8b814d67f3a0fa43ac67bead6c171fe27284699c3275
Product
Z-0065-2020

Field note

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