Device recall
Z-2476-2020: GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the…
FDA device recall · Class I · Verathon, Inc.
Key facts
| Recall number (Z-number) | Z-2476-2020 |
|---|---|
| Recall event | 85705 |
| Product | GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch Cables (Reusable Device) is ancillary equipment used with the Core 10 and Core 15 monitors. The monitor and workstation are intended to work with video… |
| Product code | CCW |
| Recalling firm | Verathon, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 22, 2024 |
| 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