Reported Apr 23, 2025 · Ongoing

Welch Allyn CP150 Electrocardiograph:

Baxter Healthcare Corporation

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Baxter Healthcare Corporation · 1 Baxter Pkwy · Deerfield, IL · 60015-4625

Is this the product you have?

  • Welch Allyn CP150 Electrocardiograph
Lot codes and dates

80 of 80 products

Products covered by this recall
Model / numberBarcodesProduct as published
CP150-2ES200732094192131All Serial Numbers. , UDI-DI: 00732094192131
CP150-2FR200732094192124UDI-DI: 00732094192124
CP150-2FR500732094192117UDI-DI: 00732094192117
CP150-2NL200732094192100UDI-DI: 00732094192100
CP150-2PT200732094192087UDI-DI: 00732094192087
CP150-2SV200732094192070UDI-DI: 00732094192070
CP150-3ENB00732094179705UDI-DI: 00732094179705
CP150-3ESB00732094179682UDI-DI: 00732094179682
CP150-4DE200732094192063UDI-DI: 00732094192063
CP150-4EN200732094179675UDI-DI: 00732094179675
CP150-4EN400732094179668UDI-DI: 00732094179668
CP150-4PT200732094192025UDI-DI: 00732094192025
CP150A-1EN200732094185157UDI-DI: 00732094185157
CP150A-1EN400732094185140UDI-DI: 00732094185140
CP150A-1EN6600732094179644UDI-DI: 00732094179644
CP150A-1ENB00732094177633UDI-DI: 00732094177633
CP150A-1ENBR00732094322415UDI-DI: 00732094322415
CP150A-1ESB00732094192230UDI-DI: 00732094192230
CP150A-1FRB00732094179637UDI-DI: 00732094179637
CP150A-2DE200732094192018UDI-DI: 00732094192018
Amount recalled
41,739 units

This recall covers 10 products

The agency filed one notice per product. You are reading one of them; the other 9 are below.

Where it was sold

  • Nationwide

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.

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.