Welch Allyn CP150 Electrocardiograph: — Class II medical device recall Z-1560-2025
Ongoing recall by Baxter Healthcare Corporation, reported 2025-04-23, distributed nationwide. There were customer reports of devices which experienced battery-related fires. The investigation found that t
| Recall number | Z-1560-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2025-03-24 |
| Classified | 2025-04-14 |
| Reported by FDA | 2025-04-23 |
| Distributed | Nationwide (US) |
| Quantity | 41,739 units |
| Reason classes | unapproved product |
| UPC / GTIN / UDI-DI | 00732094177572, 00732094177589, 00732094177596, 00732094177602, 00732094177619, 00732094177626, 00732094177633, 00732094177640, 00732094179583, 00732094179590, 00732094179606, 00732094179613, 00732094179620, 00732094179637, 00732094179644, 00732094179668, 00732094179675, 00732094179682, 00732094179705, 00732094179729, 00732094179743, 00732094179750, 00732094184815, 00732094185133, 00732094185140 and 55 more |
Product
Welch Allyn CP150 Electrocardiograph:
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1560-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.