Device recall
Z-0109-2019: Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000
FDA device recall · Class II · Besmed Health Business Corporation
Key facts
| Recall number (Z-number) | Z-0109-2019 |
|---|---|
| Recall event | 81009 |
| Product | Ambu Aura40 Standard, Reusable Laryngeal Mask Catalog Number: 340300000 |
| Product code | CAE |
| Recalling firm | Besmed Health Business Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 10, 2019 |
| FEI number | 3003256355 |
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