FDAFDA · Food and drugs·Recall number Z-1084-2024
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Published February 21, 2024 · Recall initiated: December 6, 2023
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker, Inc.
- Distributor
- US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
- Lot
- UDI: (01)00815742002386/Lot Number(s): 0000228865 0000370674
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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