# FDA recall Z-2338-2018

> **Trilliant Surgical Ltd.** · Class II · device recall initiated 2018-03-27.

## Product

Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile

## Reason for recall

Firm is voluntarily recalling cannulated driver handles (210-00-003 and 210-00-004) that may demonstrate a degradation of function with the adapter collar sticking, and/or not retaining the mating adapter male shaft.

## Distribution

U.S. States: NE, MA, GA, TX, OR, AZ, FL, OH, WA, NJ, UT, VA, CA, MN, PA, DE, OK, KS, WI, MT, IA, MO

## Key facts

- **Recall number:** Z-2338-2018
- **Recalling firm:** Trilliant Surgical Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-03-27
- **Report date:** 2018-07-11
- **Termination date:** 2020-06-04

- **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-2338-2018

## Citation

> AI Analytics. FDA recall Z-2338-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2338-2018. Source: US FDA. Licensed CC0.

---

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