Reported Feb 12, 2025 · Ongoing

IntelliVue Patient Monitor MX450. Model 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
  • Model Number866062
Lot codes and dates
  • Model Number866062
  • UDI-DI(01)00884838038769(21)
  • Serial Numbers
    • DE35169761
    • DE671V3903
    • DE671V3885
    • DE671V7898
    • DE7770DC1L
  • UDI-DI884838045859
  • Serial Numbers

    93 of 93 codes

    • DE32303399
    • DE32302479
    • DE32302480
    • DE32306956
    • DE35131294
    • DE35114613
    • DE35114612
    • DE671T9641
    • DE7770C86L
    • DE7770C86K
    • DE7770C86J
    • DE7770C86H
    • DE7770C86G
    • DE35120431
    • DE671K3731
    • DE671K3729
    • DE671K3706
    • DE671K3796
    • DE671K3816
    • DE671K3737
    • DE671K3773
    • DE671L0436
    • DE671L0462
    • DE671L0406
    • DE671L5214
    • DE671L5207
    • DE671L5206
    • DE671L5181
    • DE671L5169
    • DE671M3993
    • DE671M4048
    • DE671M4036
    • DE671M4037
    • DE671M4053
    • DE671M7009
    • DE671M7012
    • DE671M9968
    • DE671M9972
    • DE671M9963
    • DE671N0009
    • DE671N0010
    • DE671N0092
    • DE671N0008
    • DE671N0001
    • DE671N0002
    • DE671M9985
    • DE671M9999
    • DE671N0000
    • DE671P0411
    • DE671P1094
    • DE671P2457
    • DE671P2537
    • DE32306016
    • DE32306017
    • DE32306018
    • DE7580B4PC
    • DE7580B4PB
    • DE7580B4PA
    • DE7770C6ZP
    • DE7770C74Y
Amount recalled
98 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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Where this came from

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

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:38 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.