# FDA recall Z-0799-2020

> **Trilliant Surgical, LLC** · Class II · device recall initiated 2019-03-14.

## Product

Gridlock Ankle Screw Driver Bit REF 320-35-003 - Product Usage: A screwdriver facilitates implant insertion and removal.

## Reason for recall

A screwdriver used to facilitate implant insertion and removal was found to be out of specification for the minor diameter of the drive feature causing the driver to be unable to retain screws as intended.

## Distribution

US Nationwide distribution in the states of CO, CT, IA, TX and WI.    OUS: None

## Key facts

- **Recall number:** Z-0799-2020
- **Recalling firm:** Trilliant Surgical, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-14
- **Report date:** 2020-01-22
- **Termination date:** 2022-03-16

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0799-2020

## Citation

> AI Analytics. FDA recall Z-0799-2020. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-0799-2020. Source: US FDA. Licensed CC0.

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