# FDA recall Z-1925-2023

> **TELEFLEX LLC** · Class I · device recall initiated 2023-05-25.

## Product

Endotracheal Tube oral/nasal uncuffed/plain - Magill, REF 100380025

## Reason for recall

Reports of disconnection of the 15mm connector from the endotracheal tube (ET tube) for the affected products.

## Distribution

US Nationwide distribution including Puerto Rico.

## Key facts

- **Recall number:** Z-1925-2023
- **Recalling firm:** TELEFLEX LLC
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-25
- **Report date:** 2023-07-05

- **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-1925-2023

## Citation

> AI Analytics. FDA recall Z-1925-2023. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-1925-2023. Source: US FDA. Licensed CC0.

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