Z-1559-2025 Class II Ongoing
FDA device recall Z-1559-2025 was initiated by Baxter Healthcare Corporation on Mar 24, 2025 and is designated Class II. 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… The recall status is ongoing. Affected quantity: 114,202 units.
Recall details
- Product Type
- Devices
- Report Date
- Apr 23, 2025
- Initiation Date
- Mar 24, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 114,202 units
Product description
Welch Allyn CONNEX Accessory Power Management Stand:
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.
Distribution pattern
Worldwide - US Nationwide distribution.
Code information
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;
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-1559-2025
- openFDA file date
- Nov 10, 2026
- Loaded by RegDataLab
- Nov 11, 2026