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Baxter Healthcare Corporation recalls Welch Allyn CP150 Electrocardiograph:
Recalled April 23, 2025 · FDA recall Z-1560-2025 · Baxter Healthcare
Hazard
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. · FDA Class II
Units
41,739 units
Sold at
Worldwide - US Nationwide distribution.
Description
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.
Product
Welch Allyn CP150 Electrocardiograph:
Manufacturer(s)
Baxter Healthcare Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →