FDAMarch 24, 2025device

Welch Allyn CP150 Electrocardiograph:

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

baxter healthcarebaxter

UPCs

007320941921310073209419212400732094192117007320941921000073209419208700732094192070007320941797050073209417968200732094192063007320941796750073209417966800732094192025

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Welch Allyn CP150 Electrocardiograph: — Recall Details · AllClear