Philips North America Llc recalls IntelliVue Patient Monitor MX750. Product Number: 866471.
- Recall date
- October 31, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-0868-2026
- FDA classification
- Class II
- Brand / firm
- Philips North America Llc
- Sold / distributed
- Worldwide distribution - US Nationwide and the countries of Afghanistan, Albania, Algeria, Angola, Argentina, Armenia, Aruba, Australia, Austria, Azerbaijan, Bahrain, Bangladesh, Belgium, Bolivia, Bosnia, Botswana, Brazil, Brunei, Bulgaria, Burundi, Cambodia, Canada, Cayman Islands, Chile, China, C…
Why it was recalled
Potential issue where the IntelliVue monitors did not alarm.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
IntelliVue Patient Monitor MX750. Product Number: 866471.
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