Welch Allyn CP150 Electrocardiograph recalled over fire hazard
- Recall date
- March 24, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph:
- Recall number
- Z-1560-2025
- FDA classification
- Class II
- Brand / firm
- Baxter Healthcare Corporation
- Sold / distributed
- Worldwide - US Nationwide distribution.
Why it was recalled
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.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Welch Allyn CP150 Electrocardiograph:
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