Device recall
Z-0322-03: Computed Tomography system, Diagnostic Imaging: Somatom Sensation 4 Somatom…
FDA device recall · Class II · Siemens Medical Systems Inc
Key facts
| Recall number (Z-number) | Z-0322-03 |
|---|---|
| Recall event | 25075 |
| Product | Computed Tomography system, Diagnostic Imaging: Somatom Sensation 4 Somatom Volume Zoom Somatom Volume Access Somatom Balance Somatom Emotion Somatom Emotion Duo Somatom Esprit Somatom Esprit + |
| Product code | JAK |
| Recalling firm | Siemens Medical Systems Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 24, 2003 |
| 510(k) numbers | K013522 |
| FEI number | 2240869 |
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