# FDA recall Z-2546-2025

> **Encore Medical, LP** · Class II · device recall initiated 2025-07-18.

## Product

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 for recall

Their is a potential that the reamer may  kick or bind up  during or immediately prior to use.

## 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.

## Key facts

- **Recall number:** Z-2546-2025
- **Recalling firm:** Encore Medical, LP
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-18
- **Report date:** 2025-09-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Austin, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2546-2025

## Citation

> AI Analytics. FDA recall Z-2546-2025. Retrieved 2026-07-31 from https://api.ai-analytics.org/recall/Z-2546-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*