Device recall
Z-2293-2011: syngo Dynamics version 9.0, Siemens Medical Solutions, USA, Inc., Ann Arbor, MI…
FDA device recall · Class II · Siemens Medical Solutions, USA, Inc
Key facts
| Recall number (Z-number) | Z-2293-2011 |
|---|---|
| Recall event | 58545 |
| Product | syngo Dynamics version 9.0, Siemens Medical Solutions, USA, Inc., Ann Arbor, MI. The syngo Dynamics is a picture archiving and communications system intended for acceptance, transfer, display, storage, archiving and manipulation of digital medical images, including quantification and report… |
| Product code | LLZ |
| Recalling firm | Siemens Medical Solutions, USA, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 10, 2012 |
| 510(k) numbers | K102150 |
| 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