Device recall
Z-0419-2016: Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI…
FDA device recall · Class II · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-0419-2016 |
|---|---|
| Recall event | 72731 |
| Product | Hudson RCI Adult Universal Ventilator Circuit, Duel Heated Limb and Hudson RCI Adult Heated Wire Circuit Kit with Column |
| Product code | BTT |
| Recalling firm | Teleflex Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 16, 2015 |
| 510(k) numbers | K031383 |
| FEI number | 3005747797 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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