FDA Device recall Z-1559-2025
Welch Allyn CONNEX Accessory Power Management Stand
- FDA Device
- Class II
- ongoing
- Published 2025-04-23
On 2025-04-23 the FDA classified a Class II recall of Welch Allyn CONNEX Accessory Power Management Stand 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-1559-2025 |
| 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 Accessory Power Management Stand:
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: 7000-APM, UDI-DI: 00732094210613; Product Code: 75-HCA-CTB, UDI-DI: 00732094240597;…All Serial Numbers. Product Code: 7000-APM, UDI-DI: 00732094210613; Product Code: 75-HCA-CTB, UDI-DI: 00732094240597; Product Code: 75-HCA-MTB, UDI-DI: 00732094240603; |
|---|
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-1559-2025%22
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