FDA Device recall Z-2024-2012
Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent ventilatory support f…
- FDA Device
- Class I
- terminated
- Published 2012-08-01
On 2012-08-01 the FDA classified a Class I recall of Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or intermittent ventilatory support f… by Respironics, citing the specified Trilogy units are being recalled because of the potential for a faulty component in the power supply.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2024-2012 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2012-04-27 |
| Published | 2012-08-01 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Respironics |
| Distribution | AZ, CA, IL, IN, LA, MI, MN, MO, NC, NJ, NY, PA, SC, TN, TX, WI |
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.
Reason
The specified Trilogy units are being recalled because of the potential for a faulty component in the power supply.
Identifiers
| code_info | Model/Catalog Numbers: 1032800, 1040004, 1040007, 1054096, 1054260, CA1032800, R1040004, R1054655, and 1045151. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2024-2012%22
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