Device recall
Z-0420-2016: GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4…
FDA device recall · Class II · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-0420-2016 |
|---|---|
| Recall event | 72642 |
| Product | GlideScope Video Laryngoscope (GVL), Part Number GVL 3 - 0574-0007; GVL 4 - 0574-0001; GVL 5- 0574-0030. The system consists of a video laryngoscope and portable video monitor. The GlideScope Video Laryngoscopes are intended for use by qualified medical professionals to obtain a clear, unobstructed… |
| Product code | CCW |
| Recalling firm | Verathon, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 22, 2016 |
| FEI number | 3022472 |
At a glance
- None 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