Device recall
Z-0714-2024: Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2
FDA device recall · Class II · Ambu Inc.
Key facts
| Recall number (Z-number) | Z-0714-2024 |
|---|---|
| Recall event | 93599 |
| Product | Ambu aView 2 A Monitor, Catalog numbers 405011000 and 405011000US2 |
| Product code | EOQ |
| Recalling firm | Ambu Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K223299 |
| FEI number | 1121788 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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