Drug recall
syngo Dynamics Version 9.5
FDA recall event 62581 · Class II · Siemens Medical Solutions, USA, Inc
Key facts
| Event ID | 62581 |
|---|---|
| Recall numbers | Z-2219-2012 |
| Recalling firm | Siemens Medical Solutions, USA, Inc |
| Product type | Devices |
| Products | syngo Dynamics Version 9.5 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | If multiple uncompressed images/clips are sent to the syngo Dynamics server, around the same time, it is possible for an image from a patient to be placed in another patient's study. |
| Initiation date | Jul 13, 2012 |
| Report date | Aug 29, 2012 |
| Termination date | Jul 15, 2013 |
| City | Ann Arbor |
| State | MI |
| Country | United States |
| FEI number | 3003304172 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: