# FDA recall Z-1956-2019

> **Centurion Medical Products Corporation** · Class I · device recall initiated 2019-06-07.

## Product

Sheridan Endotracheal Tube contained inside Centurion kit code TC7855.

## Reason for recall

Centurion is conducting a sub-recall for Teleflex Sheridan branded Endotracheal Tracheal Tubes due to increased incidence of Sheridan connector becoming disconnected from Endotracheal Tube.

## Distribution

Distributed to one account in Arkansas.

## Key facts

- **Recall number:** Z-1956-2019
- **Recalling firm:** Centurion Medical Products Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-06-07
- **Report date:** 2019-08-07
- **Termination date:** 2020-07-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Williamston, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1956-2019

## Citation

> AI Analytics. FDA recall Z-1956-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1956-2019. Source: US FDA. Licensed CC0.

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