Device recall
Z-2099-2019: Inovo Single Luman Conserver Product Usage: This device is intended to regulate…
FDA device recall · Class II · Inovo, Inc
Key facts
| Recall number (Z-number) | Z-2099-2019 |
|---|---|
| Recall event | 82793 |
| Product | Inovo Single Luman Conserver Product Usage: This device is intended to regulate the flow of oxygen from an oxygen tank and only deliver oxygen as the patient inhales, resulting in greater efficiency and cost saving ratios. |
| Product code | NFB |
| Recalling firm | Inovo, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 2, 2021 |
| 510(k) numbers | K060751 |
| FEI number | 3000719543 |
At a glance
- 1–9 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