# FDA recall Z-1402-2023

> **Medacta Usa Inc** · Class II · device recall initiated 2023-03-08.

## Product

MectaLIF ANTERIOR - Lag Plate Flush H14, REF 03.30.302, interbody fusion device

## Reason for recall

There is a potential for breakage of the small screw used to affix the anti-backout plate.

## Distribution

US:  ID, TX, GA, VA, AZ

## Key facts

- **Recall number:** Z-1402-2023
- **Recalling firm:** Medacta Usa Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2023-03-08
- **Report date:** 2023-04-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Memphis, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1402-2023

## Citation

> AI Analytics. FDA recall Z-1402-2023. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1402-2023. Source: US FDA. Licensed CC0.

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