Device recall
Z-1035-2016: GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video…
FDA device recall · Class I · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-1035-2016 |
|---|---|
| Recall event | 73014 |
| Product | GlideScope Titanium Single-Use Video Laryngoscope. It is a single-use video laryngoscope system (GlideScope Titanium System) consists of a sterile-packaged, single-use video laryngoscope, multi-use Smart Cable and portable GlideScope video monitor. The system incorporates a high-resolution… |
| Product code | CCW |
| Recalling firm | Verathon, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 1, 2017 |
| 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