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
Reported: September 17, 2025 Initiated: July 18, 2025 #Z-2548-2025
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.
Details
- Recalling Firm
- Encore Medical, LP
- Units Affected
- 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.
- Location
- Austin, TX
Frequently Asked Questions
What product was recalled? ▼
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. Recalled by Encore Medical, LP. Units affected: 447 units.
Why was this product recalled? ▼
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 17, 2025. Severity: Moderate. Recall number: Z-2548-2025.
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