FDA Device recall Z-0532-2024
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204
- FDA Device
- Class II
- ongoing
- Published 2023-12-20
On 2023-12-20 the FDA classified a Class II recall of RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204 by Encore Medical, citing coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0532-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-09-06 |
| Published | 2023-12-20 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Encore Medical |
| Distribution | AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, PR, RI, SC, TN, TX, VA, WA |
Product
RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.
Reason
Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver
Identifiers
| code_info | Part Number: 508-32-204 UDI-DI Code: 00888912144391 Serial Numbers: 769P2825, 769P2846, 769P2893 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0532-2024%22
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