Device recall
Z-2628-2023: Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live…
FDA device recall · Class II · Ambu Inc.
Key facts
| Recall number (Z-number) | Z-2628-2023 |
|---|---|
| Recall event | 92886 |
| Product | Ambu aView 2 A Monitor-The Ambu aView 2 Advance is intended to display live imaging data from compatible Ambu visualization devices, portable endoscopy system. Catalog No: 405011000 |
| Product code | FEM |
| Recalling firm | Ambu Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1121788 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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