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

Recalled December 20, 2023 · FDA recall Z-0532-2024 · Encore Medical

Hazard

Coating hex did not engage with the Straight Mod Hexdriver or with the Hex Head Screw Driver · FDA Class II

Units

146 units

Sold at

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

Description

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

Product

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

Manufacturer(s)

Encore Medical, LP

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →