Device recall
Z-2102-2025: i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope…
FDA device recall · Class I · Intersurgical Inc
Key facts
| Recall number (Z-number) | Z-2102-2025 |
|---|---|
| Recall event | 97121 |
| Product | i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy. |
| Product code | CCW |
| Recalling firm | Intersurgical Inc |
| Recall class | Class I |
| Status | Open, Classified |
| FEI number | 1000120301 |
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