# FDA recall Z-1038-2025

> **Zimmer, Inc.** · Class II · device recall initiated 2025-01-06.

## Product

NexGen LCCK Legacy Articular Surface with Locking Screw - Striped Purple/C,D - Height 14 mm, Item Number 00-5994-022-14

## Reason for recall

It was identified internally that two commingle events occurred where the metal support post within the polyethylene articular surface was assembled incorrectly for three units within the scope.

## Distribution

Worldwide - US Nationwide distribution in the states of CA, FL, GA, KS, MO, NE, NJ, PA, TN and the countries of CHINA, INDIA, KOREA, MALAYSIA, NETHERLANDS, SINGAPORE, TAIWAN.

## Key facts

- **Recall number:** Z-1038-2025
- **Recalling firm:** Zimmer, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-06
- **Report date:** 2025-02-05

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Warsaw, IN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1038-2025

## Citation

> AI Analytics. FDA recall Z-1038-2025. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1038-2025. Source: US FDA. Licensed CC0.

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