# FDA recall Z-1924-2020

> **Wright Medical Technology Inc** · Class II · device recall initiated 2020-04-09.

## Product

WRIGHT INBONE Tibial Tray, Size: 2, Plasma Spray, Left, REF 2000252902 - Product Usage: is intended to give a patient limited mobility by reducing pain, restoring alignment and replacing the flexion and extension movement in the ankle joint.

## Reason for recall

One lot of INBONE Tibial Trays is missing the plasma coating.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-1924-2020
- **Recalling firm:** Wright Medical Technology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-09
- **Report date:** 2020-05-13
- **Termination date:** 2020-11-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1924-2020

## Citation

> AI Analytics. FDA recall Z-1924-2020. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-1924-2020. Source: US FDA. Licensed CC0.

---

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