stryker Tornier Perform Reversed Augmented Glenoid Lateralized… — Class II medical device recall Z-0113-2024
Ongoing recall by Tornier, Inc, reported 2023-10-25, distributed in CA, CO, IL, MA, MN, NC, OR, RI…. One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spac
| Recall number | Z-0113-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tornier, Inc, Bloomington, MN, United States |
| Recall initiated | 2023-09-15 |
| Classified | 2023-10-13 |
| Reported by FDA | 2023-10-25 |
| Distributed | CA, CO, IL, MA, MN, NC, OR, RI, SC, TN |
| Quantity | 30 units |
| UPC / GTIN / UDI-DI | 10846832062017 |
| Lot numbers | 1756123 |
| Model numbers | DWJ502 |
Product
stryker Tornier Perform Reversed Augmented Glenoid Lateralized Baseplate, 25mm, Offset +3mm, REF DWJ502
Reason for recall
One lot of Tournier Perform Reversed Lateralized Baseplates were found to have been manufactured with 6mm spacers instead of 3mm spacers. This nonconformance prevents the central screw from being able to thread into the baseplate.
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-0113-2024. 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.