RSP Glenoid Baseplate — Class II medical device recall Z-0532-2024
Ongoing recall by Encore Medical, LP, reported 2023-12-20, distributed in AZ, CA, FL, IN, KS, KY, ME, MN…. Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
| Recall number | Z-0532-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Encore Medical, LP, Austin, TX, United States |
| Recall initiated | 2023-09-06 |
| Classified | 2023-12-12 |
| Reported by FDA | 2023-12-20 |
| Distributed | AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, PR, RI, SC, TN, TX, VA, WA |
| Quantity | 146 units |
| UPC / GTIN / UDI-DI | 00888912144391 |
| Serial numbers | 769P2825, 769P2846, 769P2893 |
| Model numbers | 508-32-204 |
Product
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
Reason for recall
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
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-0532-2024. 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.