Philips North America Llc 2025-12-10 Health serious FDA
Health · FDA · Recall #FDA-Z-0852-2026
IntelliVue MP30. Product Number: M8002A. Recall
Issued December 10, 2025 · Philips North America Llc
In December 2025, Philips North America Llc recalled the IntelliVue MP30. Product Number: M8002A., a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Potential issue where the IntelliVue monitors did not alarm.
What you should do
- 1 Stop using IntelliVue MP30. Product Number: M8002A. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America Llc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Philips North America Llc
- Category
- Health
- Recall date
- December 10, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the countries of Afghanistan, Albania, Algeria, Angola, Argentina, Armenia, Aruba, Australia, Aus
- Recall number
- FDA-Z-0852-2026
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America Llc has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.