Device recall
Z-1408-2010: The BleaseSirius and BleaseFocus Anaesthesia Systems.
FDA device recall · Class II · Blease Medical Equipment, Ltd.
Key facts
| Recall number (Z-number) | Z-1408-2010 |
|---|---|
| Recall event | 55177 |
| Product | The BleaseSirius and BleaseFocus Anaesthesia Systems. |
| Product code | BSZ |
| Recalling firm | Blease Medical Equipment, Ltd. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2011 |
| 510(k) numbers | K051629 |
| FEI number | 3002806541 |
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