Respironics, Inc.: Medical Device Recall in 2012 - (Recall #: Z-2024-2012)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2012.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class I

Date Initiated: April 27, 2012

Date Posted: August 1, 2012

Recall Number: Z-2024-2012

Event ID: 62393

Reason for Recall:

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

Status: Terminated

Product Quantity: 173

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.

Voluntary or Mandated:

Voluntary: Firm initiated