# FDA recall Z-0484-2021

> **Hill-Rom Manufacturing, Inc.** · Class II · device recall initiated 2020-11-12.

## Product

Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.

## Reason for recall

Under certain conditions, there is a risk for fire.

## Distribution

US Nationwide distribution including in the states of AR, AZ, CA, DE, FL, IL, IN, KY, MN, NC, NM, NV, NY, OH, OK, TX, UT, VA, VT, WI.

## Key facts

- **Recall number:** Z-0484-2021
- **Recalling firm:** Hill-Rom Manufacturing, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-11-12
- **Report date:** 2020-12-02
- **Termination date:** 2022-11-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Saint Paul, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0484-2021

## Citation

> AI Analytics. FDA recall Z-0484-2021. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0484-2021. Source: US FDA. Licensed CC0.

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