# FDA recall Z-2728-2020

> **TELEFLEX MEDICAL INC** · Class II · device recall initiated 2020-07-06.

## Product

Rusch Greenlite Product Code: 004550004  GTIN: 14026704663085 (each) - Product Usage:   The laryngoscope is a device intended to allow direct visualization of the laryngeal structure and is used during tracheal intubation.

## Reason for recall

Breaking at the point of a welded joint

## Distribution

US Nationwide distribution including in the states of FL, KY, CA, ND, UT, MA, MD, AZ, MS, TX, MI, WV, AL, MO, SC, VA, AR, PA, OK, NV, NM, NE, IN, IA, NY, GA, NJ, MN, IL, NC, NH, TN, ID, CO, HI, MT, OR, ME, CT, LA, OH, RI, SD, WA, DC, KS, AK.

## Key facts

- **Recall number:** Z-2728-2020
- **Recalling firm:** TELEFLEX MEDICAL INC
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-07-06
- **Report date:** 2020-08-05
- **Termination date:** 2023-08-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Morrisville, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2728-2020

## Citation

> AI Analytics. FDA recall Z-2728-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2728-2020. Source: US FDA. Licensed CC0.

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