FDA Device recall Z-1560-2025
Welch Allyn CP150 Electrocardiograph
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Welch Allyn CP150 Electrocardiograph by Baxter Healthcare, citing 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 batte….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1560-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-03-24 |
| Published | 2025-04-23 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
Welch Allyn CP150 Electrocardiograph:
Reason
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.
Identifiers
| code_info | All Serial Numbers. Product Code: CP150-2ES2, UDI-DI: 00732094192131; Product Code: CP150-2FR2, UDI-DI: 00732094192124…All Serial Numbers. Product Code: CP150-2ES2, UDI-DI: 00732094192131; Product Code: CP150-2FR2, UDI-DI: 00732094192124; Product Code: CP150-2FR5, UDI-DI: 00732094192117; Product Code: CP150-2NL2, UDI-DI: 00732094192100; Product Code: CP150-2PT2, UDI-DI: 00732094192087; Product Code: CP150-2SV2, UDI-DI: 00732094192070; Product Code: CP150-3ENB, UDI-DI: 00732094179705; Product Code: CP150-3ESB, UDI-DI: 00732094179682; Product Code: CP150-4DE2, UDI-DI: 00732094192063; Product Code: CP150-4EN2, UDI-DI: 00732094179675; Product Code: CP150-4EN4, UDI-DI: 00732094179668; Product Code: CP150-4PT2, UDI-DI: 00732094192025; Product Code: CP150A-1EN2, UDI-DI: 00732094185157; Product Code: CP150A-1EN4, UDI-DI: 00732094185140; Product Code: CP150A-1EN66, UDI-DI: 00732094179644; Product Code: CP150A-1ENB, UDI-DI: 00732094177633; Product Code: CP150A-1ENBR, UDI-DI: 00732094322415; Product Code: CP150A-1ESB, UDI-DI: 00732094192230; Product Code: CP150A-1FRB, UDI-DI: 00732094179637; Product Code: CP150A |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1560-2025%22
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