# FDA recall Z-0885-2025

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2024-12-20.

## Product

Welch Allyn, Inc., Life2000 Ventilation System, REF BT-20-0002A

## Reason for recall

There is an issue with the ventilator battery charger that could lead to an audible and visual alarm. If the alarm is engaged, the ventilator becomes inoperable.

## Distribution

US, Nationwide Distribution

## Key facts

- **Recall number:** Z-0885-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-12-20
- **Report date:** 2025-01-22

- **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-0885-2025

## Citation

> AI Analytics. FDA recall Z-0885-2025. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-0885-2025. Source: US FDA. Licensed CC0.

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