Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER SLEEVE Model/Catal...

FDA Recall #Z-2548-2025 — Class II — July 18, 2025

Recall #Z-2548-2025 Date: July 18, 2025 Classification: Class II Status: Ongoing

Product Description

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.

Recalling Firm

Encore Medical, LP — Austin, TX

Classification

Class II — May cause temporary or medically reversible adverse health consequences.

Product Type

Devices

Product Quantity

447 units

Distribution

US Nationwide distribution in the states of AL, AZ, CA, CO, FL, HI, IA, IL, IN, KS, KY, LA, MD, ME, NE, NJ, NY, OH, PR, RI, SC, TN, TX, UT, VA, WA, WI.

Code Information

Lot Code: All Lots GTIN: 00190446843818

Status

Ongoing

Voluntary / Mandated

Voluntary: Firm initiated