Stryker Neurovascular — Class II medical device recall Z-1085-2024
Ongoing recall by Stryker, Inc., reported 2024-02-21, distributed nationwide. The microcatheter IFU contains an intended use that has not been evaluated by the FDA.
| Recall number | Z-1085-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker, Inc., Salt Lake City, UT, United States |
| Recall initiated | 2023-12-06 |
| Classified | 2024-02-14 |
| Reported by FDA | 2024-02-21 |
| Distributed | Nationwide (US) |
| Quantity | 63 units |
| UPC / GTIN / UDI-DI | 07613327313956 |
| Lot numbers | 0000136913, 0000144331, 0000163582, 0000164440, 0000182275, 0000230955, 0000240597, 0000244845, 0000370674 |
| Model numbers | 0.021IN, 90338, X162CM |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1085-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.