Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
Reported: February 21, 2024 Initiated: December 6, 2023 #Z-1084-2024
Product Description
Stryker Neurovascular, Trevo Pro 18 Microcatheter, REF 90238 0.021in X150cm
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
- 11 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 Pro 18 Microcatheter, REF 90238 0.021in X150cm. Recalled by Stryker, Inc.. Units affected: 11 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-1084-2024.
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