Device recall
Z-1556-2015: CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal…
FDA device recall · Class II · Vital Signs Colorado Inc.
Key facts
| Recall number (Z-number) | Z-1556-2015 |
|---|---|
| Recall event | 70753 |
| Product | CareFusion Vital Signs LightWand Stylet. A device inserted into an endotracheal tube to aid in the intubation procedure. |
| Product code | BSR |
| Recalling firm | Vital Signs Colorado Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 7, 2015 |
| 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