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Welch Allyn, Inc. 901049 (REF CP150S-1ENB)Recalls & reported problems

Welch Allyn, Inc. · Welch Allyn CP 150 12-Lead Resting Electrocardiograph with Spirometry; Noninterpretive, AHA ECG Cable with Disposable Electrodes, CardioPerfect Workstation Connectivity via USB and Ethernet, Color Touchscreen Display, 100-Test Memory; 3-Liter Calibration Syringe, 100–240 V, 50/60 Hz AC, IEC Plug Type-B · Class 2

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Recalls naming this device

  1. Mar 24, 2025Open, Classified

    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.

    Z-1560-2025 · Root cause: Process design · FDA record ↗

Other ELECTROCARDIOGRAPH devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.