Device recall
Z-0544-2009: Siemens syngo Dynamics Workplace, version 5.0, Siemens Medical Solutions, Ann…
FDA device recall · Class II · Siemens Medical Solutions, USA, Inc
Key facts
| Recall number (Z-number) | Z-0544-2009 |
|---|---|
| Recall event | 49457 |
| Product | Siemens syngo Dynamics Workplace, version 5.0, Siemens Medical Solutions, Ann Arbor, MI; 10090310. Intended for acceptance, transfer, display, storage, archive and manipulation of digital medical images, including quantification and report generation. |
| Product code | LLZ |
| Recalling firm | Siemens Medical Solutions, USA, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 18, 2010 |
| 510(k) numbers | K053133 |
| 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