Device recall
Z-0478-2013: The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that…
FDA device recall · Class I · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-0478-2013 |
|---|---|
| Recall event | 63635 |
| Product | The GlideScope Video Laryngoscope (GVL) is a video laryngoscope that incorporates a high-resolution color camera, an LED light source, a rechargeable lithium battery, and video output to a remote monitor. It consists of a video laryngoscope and a portable video monitor. The affected GVL and Part… |
| Product code | CCW |
| Recalling firm | Verathon, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Sep 27, 2013 |
| 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