Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V — Class II medical device recall Z-0773-2024
Ongoing recall by Tornier, Inc, reported 2024-01-31, distributed in AR, AZ, CA, CO, CT, NC, OH, TN…. The incorrect device is contained in the labeled package.
| Recall number | Z-0773-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tornier, Inc, Bloomington, MN, United States |
| Recall initiated | 2024-01-03 |
| Classified | 2024-01-19 |
| Reported by FDA | 2024-01-31 |
| Distributed | AR, AZ, CA, CO, CT, NC, OH, TN, VA |
| Countries outside the US | AU, FR, IT |
| Quantity | 50 |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00846832091614 |
| Lot numbers | 6714AZ |
| Serial numbers | 001, 050, 6714AZ001, 6714AZ002, 6714AZ003, 6714AZ004, 6714AZ005, 6714AZ006, 6714AZ007, 6714AZ008, 6714AZ009, 6714AZ010, 6714AZ011, 6714AZ012, 6714AZ013, 6714AZ014, 6714AZ015, 6714AZ016, 6714AZ017, 6714AZ018, 6714AZ019, 6714AZ020, 6714AZ021, 6714AZ022, 6714AZ023 and 27 more |
| Model numbers | 7MM, DWJ001 |
Product
Stryker Tornier Perform Reversed Glenoid Press-Fit Short Post Ti6AI4V, REF DWJ001, L: 7mm, Cementless Sterile.
Reason for recall
The incorrect device is contained in the labeled package.
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-0773-2024. 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.