The Recall Desk

FDA (Devices) recall action 82696

Philips North America, LLC recalled 4 products on 2019-06-12

The FDA (Devices) publishes a recall like this one as 4 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 4 pages.

Products
4
Announced
2019-06-12
Critical
0
Units
—

Why these products were recalled

The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .

The agency’s own wording, quoted from the enforcement report.

1–4 of 4

  • HighFDA (Devices)··2019-06-12

    Philips IntelliVue MX40 Patient Monitor Recalled for Battery Notification Issues

    Philips is recalling IntelliVue MX40 Patient Monitors because they may fail to provide visual or audible low-battery alerts, potentially disrupting patient monitoring.

    Product
    IntelliVue MX40 Patient Monitor, Product number 865352, Service Numbers All: 453564262571, 453564262591, 453564615311, 453564615331, 453564615351, and 453564615371 Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information
    Category
    Distribution
    0 states
  • HighFDA (Devices)··2019-06-12

    Philips IntelliVue MX40 Patient Monitor Recalled for Battery Defect

    Philips is recalling IntelliVue MX40 Patient Monitors because they may experience increased power consumption and lack visual or audible notifications when in a low battery state.

    Product
    IntelliVue MX40 Patient Monitor, Product number 865350, Service # USA: 453564262491 and 453564262511 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is connecte
    Category
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    0 states
  • HighFDA (Devices)··2019-06-12

    Philips IntelliVue MX40 Patient Monitor Recalled for Battery Issues

    Philips is recalling IntelliVue MX40 Patient Monitors because they may consume excess power and fail to provide visual or audible low-battery alerts.

    Product
    IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers All other countries: 453564451791, 453564451811, 453564467721, 453564467741, 453564467761, 453564467781, 453564467801, 453564467821, 453564467841, 453564467861, 453564262531, and 453564262551 - Product Usage
    Category
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    0 states
  • HighFDA (Devices)··2019-06-12

    Philips IntelliVue MX40 Patient Monitor Recalled for Battery Notification Defects

    Philips is recalling IntelliVue MX40 Patient Monitors because they may fail to provide visual or audible alerts when the battery is low.

    Product
    IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is c
    Category
    Distribution
    0 states