Device recall
Z-1040-2010: Teleflex Medical, Hudson RCI, Concha Therm Neptune, Heated Humidifier. Product…
FDA device recall · Class II · Telefelx Medical
Key facts
| Recall number (Z-number) | Z-1040-2010 |
|---|---|
| Recall event | 54232 |
| Product | Teleflex Medical, Hudson RCI, Concha Therm Neptune, Heated Humidifier. Product numbers: 425-00, 425-10 and 525-30. |
| Product code | BTT |
| Recalling firm | Telefelx Medical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2011 |
| 510(k) numbers | K063758 |
| 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