Device recall
Z-2478-2010: Fabius GS Anesthesia Machine, OR/Anesthesia, Draeger Medical, Inc., 3135 Quarry…
FDA device recall · Class II · Draeger Medical Systems, Inc.
Key facts
| Recall number (Z-number) | Z-2478-2010 |
|---|---|
| Recall event | 56676 |
| Product | Fabius GS Anesthesia Machine, OR/Anesthesia, Draeger Medical, Inc., 3135 Quarry Road, Telford, PA 18969 inhalation anesthesia machine for use in operating, induction and recovery rooms |
| Product code | BSZ |
| Recalling firm | Draeger Medical Systems, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 23, 2011 |
| 510(k) numbers | K042419 |
| FEI number | 2510954 |
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