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Recall Observatory FDA recall evidence

Device product

Welch Allyn CONNEX Accessory Power Management Stand:

Z-1559-2025

March 24, 2025

Class II

Product summary

Firm
Baxter Healthcare Corporation
Event
Event 96478
Status
Ongoing
Classification
Class II
Quantity
114,202 units
Official record key
device-enforcement:Z-1559-2025

Official wording

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.

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;

Distribution pattern: Worldwide - US Nationwide distribution.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.