Class II

Medical Device Recall: Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm

Stryker, Inc. · December 6, 2023

Reason for Recall

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

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

63 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1085-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Stryker, Inc. Medical Device Recall: Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm | SafeCheck