Reported Jun 14, 2023 · Ongoing

Trilogy Evo Universal Ventilator, Model Number DS2000X11B

Philips Respironics, Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

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 Respironics, Inc. · 1001 Murry Ridge Ln · Murrysville, PA · 15668-8517

Is this the product you have?

  • Trilogy Evo Universal Ventilator, Model Number DS2000X11B
Lot codes and dates
  • UDI-DI606959052000
  • Serial Numbers

    2,326 of 2,326 codes

    • H27736231F4BE
    • H277362379188
    • H27736246CD09
    • H277372867812
    • H27737288916C
    • H2773729661CA
    • H27737302AA2A
    • H27737306EC0E
    • H2773730914F9
    • H27737331B2D9
    • H27737344A87C
    • H277373468B6E
    • H277373596A41
    • H277373815671
    • H2773738401DC
    • H2773740998FC
    • H277374132E7E
    • H277374212704
    • H277374525897
    • H277374740E11
    • H277374848DD9
    • H27737492F137
    • H27737496B713
    • H277375206C51
    • H277375242A75
    • H2773757677DF
    • H277375789EA1
    • H27737583A3BA
    • H27737593BA62
    • H27737607C43A
    • H27737614EF79
    • H27737624C511
    • H27737635CD40
    • H27737646B2D3
    • H27737656AB0B
    • H27737664A271
    • H2773767871C5
    • H277376870AFA
    • H27737700EA59
    • H27737702C94B
    • H277378459053
    • H27737846A2C8
    • H27737847B341
    • H27737853ECBD
    • H277378549802
    • H27737869698F
    • H277378779929
    • H277378925494
    • H277378970339
    • H2773792845BA
    • H27737966CBA4
    • H27737971A6C3
    • H277379821790
    • H2773801950BC
    • H27738021F69C
    • H277380378A72
    • H27738043815E
    • H27738052890F
    • H27738057DEA2
    • H277380680C3D
Amount recalled
22,237 devices

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Where it was sold

  • Nationwide

Why it was recalled

Stop using this product now

The Trilogy Evo Universal ventilator provides continuous or intermittent positive pressure ventilation for the care of individuals who require mechanical ventilation. Trilogy Evo Universal is intended for pediatric through adult patients weighing at least 2.5 kg. The ventilator can measure, display, record, and alarm SpO2, FiO2, CO2, and pulse rate data when integrated with the appropriate accessories. The ventilator is suitable for use in institutional and hospital settings and non-emergency transport settings; for example, wheelchair. It may be used for both invasive and non-invasive ventilation.

Using this product could cause serious injury, illness or death — stop using it now.

Want the full recall guide?

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, 6:55 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.