3910-090-800 ASSY — Class II medical device recall Z-2057-2018
Completed recall by Stryker Corporation, reported 2018-06-13, distributed in MA. Inadvertent shipment of expired units.
| Recall number | Z-2057-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Corporation, San Jose, CA, United States |
| Recall initiated | 2017-12-21 |
| Classified | 2018-06-01 |
| Reported by FDA | 2018-06-13 |
| Distributed | MA |
| UPC / GTIN / UDI-DI | 07613327055795 |
| Lot numbers | 14239AG2 |
Product
3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box. The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.
Reason for recall
Inadvertent shipment of expired units.
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-2057-2018. 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.