Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever — Class II medical device recall Z-0347-2018
Terminated recall by Stryker Neurovascular, reported 2018-01-24. Stryker Neurovascular has become aware that at least 1 (one) Trevo XP Provue System was manufactured where the
| Recall number | Z-0347-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Neurovascular, Fremont, CA, United States |
| Recall initiated | 2017-11-28 |
| Classified | 2018-01-14 |
| Reported by FDA | 2018-01-24 |
| Terminated | 2020-04-28 |
| Lot numbers | 63034 |
| Model numbers | 80052 |
Product
Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
Reason for recall
Stryker Neurovascular has become aware that at least 1 (one) Trevo XP Provue System was manufactured where the carton sleeve did not match the physical contents of the pack.
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-0347-2018. 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.