Device recall
Z-0811-2016: GlideScope Video Laryngoscope Reusable Blades (GVL 3, 4, 5 and AVL 2, 3, 4, 5)…
FDA device recall · Class II · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-0811-2016 |
|---|---|
| Recall event | 71008 |
| Product | GlideScope Video Laryngoscope Reusable Blades (GVL 3, 4, 5 and AVL 2, 3, 4, 5). GVL: The GlideScope Video Laryngoscope 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… |
| Product code | CCW |
| Recalling firm | Verathon, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 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