Device recall
Z-1235-06: KinetDx 4.0 Ultrasound Image Management System.
FDA device recall · Class III · Siemens Medical Solutions, USA, Inc
Key facts
| Recall number (Z-number) | Z-1235-06 |
|---|---|
| Recall event | 35043 |
| Product | KinetDx 4.0 Ultrasound Image Management System. |
| Product code | LLZ |
| Recalling firm | Siemens Medical Solutions, USA, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | May 1, 2007 |
| 510(k) numbers | K041029 |
| FEI number | 3003304172 |
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