Drug recall
Trilogy Ventilators The Respironics Trilogy 100 system provides continuous or intermittent ventilator support…
FDA recall event 67550 · Class I · Phillips Respironics, Inc.
Key facts
| Event ID | 67550 |
|---|---|
| Recall numbers | Z-1143-2014 |
| Recalling firm | Phillips Respironics, Inc. |
| Product type | Devices |
| Products | Trilogy Ventilators The Respironics Trilogy 100 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended… |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Internal testing revealed a potentially defective component on the power management board that could affect the function of certain Trilogy Ventilators resulting in loss of therapy to patients. |
| Initiation date | Feb 11, 2014 |
| Report date | Mar 12, 2014 |
| Termination date | Apr 17, 2015 |
| 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: