Drug recall
Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200…
FDA recall event 73177 · Class II · Philips Respironics
Key facts
| Event ID | 73177 |
|---|---|
| Recall numbers | Z-1065-2016 |
| Recalling firm | Philips Respironics |
| Product type | Devices |
| Products | Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin Plus Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care of… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Software Issue |
| Initiation date | Jan 18, 2016 |
| Report date | Mar 16, 2016 |
| Termination date | May 26, 2017 |
| City | Monroeville |
| State | PA |
| Country | United States |
| FEI number | 3007871739 |
At a glance
- 1–9 Products in this recall
- None 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: