Device recall
Z-1065-2016: Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202, Trilogy EC, Garbin, Garbin…
FDA device recall · Class II · Philips Respironics
Key facts
| Recall number (Z-number) | Z-1065-2016 |
|---|---|
| Recall event | 73177 |
| Product | 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 individuals who require mechanical ventilation. |
| Product code | CBK |
| Recalling firm | Philips Respironics |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 26, 2017 |
| 510(k) numbers | K083526, K093416, K093905 |
| FEI number | 3007871739 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database