Reported Feb 12, 2025 · Ongoing
IntelliVue Patient Monitor MX550. Model Number: 866066
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 MX550
- Model Number866066
- Lot codes and dates
- Model Number866066
- UDI-DI(01)00884838038783(21)
- Serial Numbers
74 of 74 codes
DE671E3020DE671E2989DE671E2988DE671E3086DE671E3085DE671E3084DE671E3097DE671E3096DE671E3095DE671E3094DE671E3093DE671E3253DE671E3246DE671E3245DE671E3244DE671E3241DE671E3240DE671E3234DE671E3235DE671E3238DE671E3239DE671E3021DE671E3236DE671E3865DE671E3863DE671E3862DE671E3861DE671E3860DE671E3859DE671E3858DE671E3857DE671E3856DE671E3855DE671E3853DE671E3852DE671E3867DE671E3871DE671E3730DE671E3729DE671E3866DE35186967DE35186949DE35186948DE35186947DE35186944DE35186943DE35186942DE35186941DE35186940DE35186939DE35186938DE35186982DE35186945DE35199396DE35199398DE35199428DE671E2030DE671H1334DE32302561DE32302562
- Amount recalled
- 74 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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