Device recall
Z-2018-2023: Oxylog 3000 Plus emergency and transport ventilator
FDA device recall · Class I · Draeger Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2018-2023 |
|---|---|
| Recall event | 92443 |
| Product | Oxylog 3000 Plus emergency and transport ventilator |
| Product code | CBK |
| Recalling firm | Draeger Medical, Inc. |
| Recall class | Class I |
| Status | Open, Classified |
| 510(k) numbers | K103625 |
| FEI number | 2517967 |
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