Device recall
Z-2454-2008: Light Wand Orotracheal Lighted Stylet, Part number: 3910. Sterile, Vital Signs…
FDA device recall · Class II · Vital Signs Colorado Inc.
Key facts
| Recall number (Z-number) | Z-2454-2008 |
|---|---|
| Recall event | 49140 |
| Product | Light Wand Orotracheal Lighted Stylet, Part number: 3910. Sterile, Vital Signs Colorado Inc., Englewood, CO. , packaged 20 per case. |
| Product code | BSR |
| Recalling firm | Vital Signs Colorado Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 10, 2011 |
| 510(k) numbers | K944729 |
| FEI number | 1718887 |
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