# FDA recall Z-0703-2020

> **Teleflex Medical** · Class II · device recall initiated 2019-10-30.

## Product

HUDSON RCI SHERIDAN SHERI-BRONCH Endobronchial Tube REF 5-16135 - Product Usage: The Sheridan Endobronchial Tubes are intended for use in Thoracic surgery, brochospirometry, adminitration of endobronchial anesthesia and other uses commonly requiring endobronchial intubation. The Sheridan Endobronchial tube is indicated for main stem bronchus intubation and allows for selective inflation or deflation of either lung.

## Reason for recall

The tracheal and brochial swivel connectors are incorrectly labeled.

## Distribution

US Nationwide distribution in the states of CT, OK, LA, IL, GA, NY, CA, MT, MI, MA, FL.

## Key facts

- **Recall number:** Z-0703-2020
- **Recalling firm:** Teleflex Medical
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-30
- **Report date:** 2019-12-25
- **Termination date:** 2021-09-30

- **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-0703-2020

## Citation

> AI Analytics. FDA recall Z-0703-2020. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0703-2020. Source: US FDA. Licensed CC0.

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