Encore Medical, LP: Medical Device Recall in 2023 - (Recall #: Z-0532-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

RSP Glenoid Baseplate, 30mm P2 Porous Coated REF 508-32-204. DJO Surgical shoulder device.

Product Classification:

Class II

Date Initiated: September 6, 2023

Date Posted: December 20, 2023

Recall Number: Z-0532-2024

Event ID: 93428

Reason for Recall:

Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver

Status: Ongoing

Product Quantity: 146 units

Code Information:

Part Number: 508-32-204 UDI-DI Code: 00888912144391 Serial Numbers: 769P2825, 769P2846, 769P2893

Distribution Pattern:

U.S.: AZ, CA, FL, IN, KS, KY, ME, MN, MS, NJ, OH, Puerto Rico, RI, SC, TN, TX, VA, and WA O.U.S.: None

Voluntary or Mandated:

Voluntary: Firm initiated