Stryker — Class II medical device recall Z-0287-2024
Ongoing recall by Stryker Corporation, reported 2023-11-15, distributed in MN, NH, NJ, NY, OH, TX. Expired product distributed
| Recall number | Z-0287-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Corporation, San Jose, CA, United States |
| Recall initiated | 2023-09-13 |
| Classified | 2023-11-09 |
| Reported by FDA | 2023-11-15 |
| Distributed | MN, NH, NJ, NY, OH, TX |
| Quantity | 19 kits |
| UPC / GTIN / UDI-DI | 07613252632863 |
| Lot numbers | 007047 |
| Model numbers | 00241 |
Product
Stryker, REF: CAT00241, Portal Entry Kit consisting of a skin marker, disposable ruler, (2) FlexSticks, 30 ml syringe, and (2) 17 Ga Needles. Used to aid the surgeon in establishing arthroscopic portals and joint access.
Reason for recall
Expired product distributed
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-0287-2024. 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.