# FDA recall Z-2796-2020

> **Wright Medical Technology, Inc.** · Class II · device recall initiated 2020-07-28.

## Product

Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a range of k-wires to assist in removal of cannulated screws. This product is a multiple use, non-sterile instrument.

## Reason for recall

Hardware removal kit does not include drivers to remove Dart-Fire 2.5 and 3.0mm Headless screws.

## Distribution

US Nationwide distribution including in the states of CO, TX, OR, KX, SC, CA, AR, NJ, UT, VA, MO, NC, FL, IL.

## Key facts

- **Recall number:** Z-2796-2020
- **Recalling firm:** Wright Medical Technology, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-28
- **Report date:** 2020-08-19
- **Termination date:** 2022-11-16

- **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-2796-2020

## Citation

> AI Analytics. FDA recall Z-2796-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2796-2020. Source: US FDA. Licensed CC0.

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