Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
Reported: February 21, 2024 Initiated: December 6, 2023 #Z-1085-2024
Product Description
Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm
Reason for Recall
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Details
- Recalling Firm
- Stryker, Inc.
- Units Affected
- 63 units
- Distribution
- US Nationwide distribution in the states of AL, FL, GA, HI, IL, MI, NC, NH, OH, PA, TX, VA.
- Location
- Salt Lake City, UT
Frequently Asked Questions
What product was recalled? ▼
Stryker Neurovascular, Trevo Trak 21 Microcatheter, REF 90338, 0.021in X162cm. Recalled by Stryker, Inc.. Units affected: 63 units.
Why was this product recalled? ▼
The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on February 21, 2024. Severity: Moderate. Recall number: Z-1085-2024.
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