Reported Feb 12, 2025 · Ongoing
IntelliVue Patient Monitor MX500. Model Number: 866064
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 MX500
- Model Number866064
- Lot codes and dates
- Model Number866064
- UDI-DI(01)00884838038776(21)
- Serial Numbers
DE7580A1R5DE7580A1R4DE7580A1R1DE7580A1R0DE7580A1PMDE7580A1PLDE7580A1PKDE7580A1PJDE7580A1P5DE351C8913DE351C8912DE351C8908DE351C8911DE351C8910DE351C8909DE32300881DE32300882DE32300883DE32300937DE32300936DE32301099DE35114607DE35114606DE671T0786DE671K1669DE671V9213DE35133301DE671N0625DE671E0967DE671E0964DE671E0965DE671E0968DE671E0978DE671E1009DE671E1008DE671E1007DE671E1006DE671E1005DE671E1004DE671E0977DE671E1003DE671E0979DE671E1015DE671E0966DE671E1059
- Amount recalled
- 45 units
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
This product could cause temporary or reversible health problems — stop using it.
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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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