Welch Allyn, Inc. 901049 (REF CP150A-1FRB)Recalls & reported problems
Welch Allyn, Inc. · Welch Allyn CP 150 12-Lead Resting Electrocardiograph with Automatic ECG Interpretation, AHA ECG Cable with Disposable Electrodes, CardioPerfect Workstation Connectivity via USB and Ethernet, Color Touchscreen Display, 100-Test Memory; 100–240 V, 50/60 Hz AC, IEC Plug Type-B; French Language · 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.
1 other recall cover devices cleared under the same FDA submission (K141582); they may or may not involve this specific model.
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
- 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 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K141582. One submission often covers many models, so check the product and lot details in each record.
- Z-2323-2024 · Jun 3, 2024 · Open, ClassifiedWelch Allyn CP150 Electrocardiograph with Spirometry Option, Product Code: CP150A-1ENB. The Electrocardiograph is one of the tools that clinicians use to evaluate, diagnose, and mo
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.