FDA-Device2025-04-23Class II
Welch Allyn Connex Vital Signs Monitor (CVSM):
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.
Sold states
Worldwide - US Nationwide distribution.
Affected count
228,412 units
Manufactured in
1 Baxter Pkwy, Deerfield, IL, United States
Products
Welch Allyn Connex Vital Signs Monitor (CVSM):
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1558-2025More Baxter Healthcare Corporation recalls
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT KIT AC recalled for nebulizer cup leakage risk
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- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT 5KIT AC recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Hillrom VOLARA System P.CIRCUIT KIT recalled for nebulizer cup leakage risk
- FDA-Device2026-07-08Hillrom Volara P.Circuit 5Kit breathing device recalled for nebulizer cup leakage risk
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