# FDA recall Z-1725-2025

> **Baxter Healthcare Corporation** · Class I · device recall initiated 2025-04-07.

## Product

Welch Allyn Life2000 Ventilation system, Product Codes:    1)	BT-20-0002;   2)	BT-20-0002A;   3)	BT-20-0002AP;   4)	BT200007;   5)	BT-20-0007;   6)	BT200011;   7)	BT-20-0011;   8)	RMS010118CP.

## Reason for recall

A cybersecurity vulnerability was discovered through internal testing.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1725-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-04-07
- **Report date:** 2025-05-21

- **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-1725-2025

## Citation

> AI Analytics. FDA recall Z-1725-2025. Retrieved 2026-08-02 from https://api.ai-analytics.org/recall/Z-1725-2025. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*