FDA Enforcement
Class II
Ongoing
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311 Product Description: Material: S.S/Nitronic, Non-Sterile
Recall: Z-2546-2025
·
Reported September 17, 2025
Enforcement
- Recall Number
- Z-2546-2025
- Event ID
- 97412
- Classification
- Class II
- Status
- Ongoing
- Product Type
- Devices
- Firm
- Encore Medical, LP
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Report Date
- September 17, 2025
- Initiation Date
- July 18, 2025
- Classification Date
- September 10, 2025
- Address
- 9800 Metric Blvd, N/A, Austin, TX, 78758-5445, United States
Description
Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311 Product Description: Material: S.S/Nitronic, Non-Sterile
Reason
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
Code Info
Lot Code: Item Number: All Lots GTIN: 00190446843825
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.
Quantity
927 units