Device recall
Z-0291-2007: Datex Ohmeda Compact Absorber, Disposable, REF 427002100, white to violet and…
FDA device recall · Class II · Datex - Ohmeda, Inc
Key facts
| Recall number (Z-number) | Z-0291-2007 |
|---|---|
| Recall event | 36326 |
| Product | Datex Ohmeda Compact Absorber, Disposable, REF 427002100, white to violet and REF 427002000, Pink to white. Used with GE Healthcare ADU anesthesia systems. GE Healthcare Finland Oy, Helsinki, Finland +358 10 39411. |
| Product code | BSZ |
| Recalling firm | Datex - Ohmeda, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 17, 2011 |
| 510(k) numbers | K973985 |
| FEI number | 2183066 |
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