Class II

Medical Device Recall: Welch Allyn Connex Vital Signs Monitor (CVSM):

Baxter Healthcare Corporation · March 24, 2025

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

Worldwide - US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

228,412 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1558-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Baxter Healthcare Corporation Medical Device Recall: Welch Allyn Connex Vital Signs Monitor (CVSM): | SafeCheck