Device recall
Z-0296-2012: Trilogy 100, 200 and 202 Ventilators The device is intended to be used in home…
FDA device recall · Class I · Respironics, Inc.
Key facts
| Recall number (Z-number) | Z-0296-2012 |
|---|---|
| Recall event | 60099 |
| Product | Trilogy 100, 200 and 202 Ventilators The device is 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. |
| Product code | CBK |
| Recalling firm | Respironics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 6, 2012 |
| 510(k) numbers | K083526 |
| FEI number | 2518422 |
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