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

    • DE671E3020
    • DE671E2989
    • DE671E2988
    • DE671E3086
    • DE671E3085
    • DE671E3084
    • DE671E3097
    • DE671E3096
    • DE671E3095
    • DE671E3094
    • DE671E3093
    • DE671E3253
    • DE671E3246
    • DE671E3245
    • DE671E3244
    • DE671E3241
    • DE671E3240
    • DE671E3234
    • DE671E3235
    • DE671E3238
    • DE671E3239
    • DE671E3021
    • DE671E3236
    • DE671E3865
    • DE671E3863
    • DE671E3862
    • DE671E3861
    • DE671E3860
    • DE671E3859
    • DE671E3858
    • DE671E3857
    • DE671E3856
    • DE671E3855
    • DE671E3853
    • DE671E3852
    • DE671E3867
    • DE671E3871
    • DE671E3730
    • DE671E3729
    • DE671E3866
    • DE35186967
    • DE35186949
    • DE35186948
    • DE35186947
    • DE35186944
    • DE35186943
    • DE35186942
    • DE35186941
    • DE35186940
    • DE35186939
    • DE35186938
    • DE35186982
    • DE35186945
    • DE35199396
    • DE35199398
    • DE35199428
    • DE671E2030
    • DE671H1334
    • DE32302561
    • DE32302562
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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:44 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.