FDA Device recall Z-1558-2025
Welch Allyn Connex Vital Signs Monitor (CVSM)
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Welch Allyn Connex Vital Signs Monitor (CVSM) 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-1558-2025 |
| 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 Connex Vital Signs Monitor (CVSM):
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: 67MCTX-4, UDI-DI: 00732094193787; Product Code: 67MCTX-6, UDI-DI: 00732094194654; Pr…All Serial Numbers. Product Code: 67MCTX-4, UDI-DI: 00732094193787; Product Code: 67MCTX-6, UDI-DI: 00732094194654; Product Code: 67MCTX-B, UDI-DI: 00732094151367; Product Code: 67MCXP-B, UDI-DI: 00732094151350; Product Code: 67MCXX-B, UDI-DI: 00732094151343; Product Code: 67MREP-B, UDI-DI: 00732094151336; Product Code: 67MREX-B, UDI-DI: 00732094151329; Product Code: 67MRTP-B, UDI-DI: 00732094151312; Product Code: 67MRTX-B, UDI-DI: 00732094151305; Product Code: 67MRXP-4, UDI-DI: 00732094193640; Product Code: 67MRXP-B, UDI-DI: 00732094151299; Product Code: 67MRXX-B, UDI-DI: 00732094151282; Product Code: 67MSTP-6, UDI-DI: 00732094194548; Product Code: 67MSTP-B, UDI-DI: 00732094177541; Product Code: 67MSTX-6, UDI-DI: 00732094194531; Product Code: 67MSTX-B, UDI-DI: 00732094177558; Product Code: 67MXDX-B, UDI-DI: 00732094249163; Product Code: 67MXEP-2, UDI-DI: 00732094193619; Product Code: 67MXEP-4, UDI-DI: 00732094193602; Product Code: 67NCEP-2, UDI-DI: 00732094193497; Product Code: 67NCE |
|---|
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-1558-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.