# FDA recall Z-0371-2023

> **Bunnell, Inc.** · Class II · device recall initiated 2022-11-02.

## Product

2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside Patient Circuit Kits, Catalog: 938

## Reason for recall

Some adaptors, for use with high frequency ventilators, were packaged improperly, and may deform at the tip, which may impair the ability to pass a suction catheter or may affect normal ventilator performance, which may lead to hypercarbia, hypoxia, and gas trapping.

## Distribution

US Nationwide Distribution: PA, NY, AR, AZ, TN, SC, MA, FL, CA, TX, MD, VA, NV, IL, IN, IA, HI, KY, LA, WI, GA, OH, MI, MO, MN, NJ, MS, NC, ND, NM, UT, OK, WA, RI;  OUS: Canada

## Key facts

- **Recall number:** Z-0371-2023
- **Recalling firm:** Bunnell, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-02
- **Report date:** 2022-12-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Salt Lake City, UT, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0371-2023

## Citation

> AI Analytics. FDA recall Z-0371-2023. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-0371-2023. Source: US FDA. Licensed CC0.

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