# FDA recall Z-1560-2025

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2025-03-24.

## Product

Welch Allyn CP150 Electrocardiograph:

## Reason for recall

There were customer reports of devices which experienced battery-related fires. The investigation found that the devices in question were utilizing third-party, after-market batteries that are not approved by Baxter.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-1560-2025
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-24
- **Report date:** 2025-04-23

- **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-1560-2025

## Citation

> AI Analytics. FDA recall Z-1560-2025. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-1560-2025. Source: US FDA. Licensed CC0.

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