Reported Dec 10, 2025 · Ongoing
IntelliVue Patient Monitor MX450. Product Number: 866062.
Philips North America LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289
Is this the product you have?
- IntelliVue Patient Monitor MX450
- Product Number866062
- Lot codes and dates
- Product Number866062
- UDI-DI00884838038769; All Serial No
- Amount recalled
- 1,913,441 units
This recall covers 24 products
The agency filed one notice per product. You are reading one of them; the other 23 are below.
11 more are in the archive.
Where it was sold
Why it was recalled
Potential issue where the IntelliVue monitors did not alarm.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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