Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID… — Class II medical device recall Z-2548-2025
Ongoing recall by Encore Medical, LP, reported 2025-09-17, distributed nationwide. Their is a potential that the reamer may kick or bind up during or immediately prior to use.
| Recall number | Z-2548-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, LP, Austin, TX, United States |
| Recall initiated | 2025-07-18 |
| Classified | 2025-09-10 |
| Reported by FDA | 2025-09-17 |
| Distributed | Nationwide (US) |
| Quantity | 447 units |
| UPC / GTIN / UDI-DI | 00190446843818 |
| Model numbers | 804-06-310 |
Product
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE Model/Catalog Number: 804-06-310 Product Description: Material: S.S/CoCrMo, Non-Sterile
Reason for recall
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
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-2548-2025. 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.