Device recall
Z-0567-2010: SeQual Technologies Inc. Eclipse Oxygen System, Model 1000 Indicated for the…
FDA device recall · Class II · Sequal Technologies Inc
Key facts
| Recall number (Z-number) | Z-0567-2010 |
|---|---|
| Recall event | 53952 |
| Product | SeQual Technologies Inc. Eclipse Oxygen System, Model 1000 Indicated for the administration of supplemental oxygen. |
| Product code | CAW |
| Recalling firm | Sequal Technologies Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 18, 2012 |
| 510(k) numbers | K013931 |
| FEI number | 1000519984 |
At a glance
- 1–9 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