Stroke Fast Pack — Class II medical device recall Z-2799-2017
Terminated recall by Stryker Neurovascular, reported 2017-08-09, distributed nationwide. Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were manufactured using a carton sle
| Recall number | Z-2799-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Neurovascular, Fremont, CA, United States |
| Recall initiated | 2017-06-26 |
| Classified | 2017-07-29 |
| Reported by FDA | 2017-08-09 |
| Terminated | 2021-03-29 |
| Distributed | Nationwide (US) |
| Quantity | 43 packages |
| Lot numbers | QPC20107530, QPC20107745, QPC20107814, QPC20110247 |
Product
Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20, Trevo Pro 14 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK32021001
Reason for recall
Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs were manufactured using a carton sleeve where the pre-printed contents on the back of the 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-2799-2017. 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.