# FDA recall Z-1726-2025

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

## Product

Welch Allyn Life2000 Compressor, Product Codes:    1)	BT-80-0004;   2)	BT-80-0004A;   3)	BT-80-0008;   4)	BT-80-0008A;   5)	RMS010093CP.

## Reason for recall

A cybersecurity vulnerability was discovered through internal testing.

## Distribution

Worldwide distribution.

## Key facts

- **Recall number:** Z-1726-2025
- **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-1726-2025

## Citation

> AI Analytics. FDA recall Z-1726-2025. Retrieved 2026-08-03 from https://api.ai-analytics.org/recall/Z-1726-2025. Source: US FDA. Licensed CC0.

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