FDAFDA · Food and drugs·Recall number Z-1559-2025
Welch Allyn CONNEX Accessory Power Management Stand:
Published April 23, 2025 · Recall initiated: March 24, 2025
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
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.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Baxter Healthcare Corporation
- Distributor
- Worldwide - US Nationwide distribution.
- Lot
- 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;
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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