Drug recall
Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy systems provides continuous or…
FDA recall event 62393 · Class I · Respironics, Inc.
Key facts
| Event ID | 62393 |
|---|---|
| Recall numbers | Z-2024-2012 |
| Recalling firm | Respironics, Inc. |
| Product type | Devices |
| Products | 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… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The specified Trilogy units are being recalled because of the potential for a faulty component in the power supply. |
| Initiation date | Apr 27, 2012 |
| Report date | Aug 1, 2012 |
| Termination date | Nov 1, 2012 |
| City | Murrysville |
| State | PA |
| Country | United States |
| FEI number | 2518422 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: