# FDA recall Z-1760-2019

> **Teleflex Medical** · Class I · device recall initiated 2019-05-24.

## Product

Hudson RCI Sheridan:  1) CF 6.0 mm, Product Codes:  5-10112, 5-10212  2) CF 6.5 mm, Product Codes:  5-10113, 5-10213  3) CF 7.0 mm, Product Codes:  5-10114, 5-10214  4) CF 7.5 mm, Product Codes:  V5-10115, 5-10115, 5-10215  5) CF 8.0 mm, Product Codes:  5-10116, 5-10216, V5-10116  6) CF 8.5 mm, Product Codes:  5-10117, 5-10217    Product Usage:  Tracheal tube/airway management

## Reason for recall

This voluntary recall is due to reported complaints (<0.0025% of all in scope distributed product) indicating that there is an increased incidence of specific lots of the 15 mm Sheridan connector becoming disconnected from the Endotracheal tube.

## Distribution

Worldwide - US Nationwide Distribution

## Key facts

- **Recall number:** Z-1760-2019
- **Recalling firm:** Teleflex Medical
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-24
- **Report date:** 2019-06-26
- **Termination date:** 2022-02-15

- **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-1760-2019

## Citation

> AI Analytics. FDA recall Z-1760-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1760-2019. Source: US FDA. Licensed CC0.

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