Reported Feb 21, 2024 · Ongoing
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Stryker, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker, Inc. · 4870 West 2100 South · Salt Lake City, UT · 84104
Is this the product you have?
Stryker NeurovascularTrevo Pro 18 MicrocatheterREF 90238 0.021in X150cm
- Lot codes and dates
- UDI(01)00815742002386/Lot
- Number(s)0000228865 0000370674
- Amount recalled
- 11 units
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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