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Recall Observatory FDA recall evidence

Device product

Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The devices are intended to be used in home, institution/hospital, and portable applications such as wheelchairs and gurneys, and may be used for both invasive and non-invasive ventilation. They are not intended to be used as a transport ventilator.

Z-2024-2012

April 27, 2012

Class I

Product summary

Firm
Respironics, Inc.
Event
Event 62393
Status
Terminated
Classification
Class I
Quantity
173
Official record key
device-enforcement:Z-2024-2012

Official wording

Reason: The specified Trilogy units are being recalled because of the potential for a faulty component in the power supply.

Code information: Model/Catalog Numbers: 1032800, 1040004, 1040007, 1054096, 1054260, CA1032800, R1040004, R1054655, and 1045151.

Distribution pattern: Worldwide Distribution - USA including AZ, CA, IL, IN, LA, MI, MN, MO, NJ, NY, NC, PA, SC, TN, TX, and WI and the countries of Canada, Denmark, Estonia, Finland, France, Great Britian, India, Italy, Japan, Korea, Saudi Arabia, and Spain.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The specified Trilogy units are being recalled because of the potential for a faulty component in the power supply.