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Recall Observatory FDA recall evidence

Device product

Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm

Z-1084-2024

December 06, 2023

Class II

Product summary

Firm
Stryker, Inc.
Event
Event 93678
Status
Ongoing
Classification
Class II
Quantity
11 units
Official record key
device-enforcement:Z-1084-2024

Official wording

Reason: The microcatheter IFU contains an intended use that has not been evaluated by the FDA.

Code information: UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674

Distribution pattern: US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The microcatheter IFU contains an intended use that has not been evaluated by the FDA.