# FDA recall Z-2140-2024

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2024-05-29.

## Product

Life2000 Ventilator, Product Code: MS-01-0118, which is contained in the Life2000 Ventilator System, with Product Codes BT-20-0002, BT-20-0002A and BT-20-0002AP.     The Life2000 ventilation system includes the Life2000 ventilator which has its individual label.

## Reason for recall

Potential for certain Life2000 ventilator systems to either fail to charge or have intermittent charging behavior due to damage to the battery charger dongle. Damage of the battery charger dongle prevents the ventilator's internal battery from charging.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2140-2024
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-29
- **Report date:** 2024-07-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2140-2024

## Citation

> AI Analytics. FDA recall Z-2140-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2140-2024. Source: US FDA. Licensed CC0.

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