Device recall
Z-2024-2012: Respironics Trilogy 100, 200, and 202 Ventilators The Respironics Trilogy…
FDA device recall · Class I · Respironics, Inc.
Key facts
| Recall number (Z-number) | Z-2024-2012 |
|---|---|
| Recall event | 62393 |
| Product | 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 ventilation. Trilogy 100 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The… |
| Product code | CBK |
| Recalling firm | Respironics, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 1, 2012 |
| 510(k) numbers | K083526, K093416, K093905 |
| 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