Drug recall
Syngo Dynamics; Kinetdx Picture Archiving and Communications System
FDA recall event 73907 · Class II · Siemens Medical Solutions USA, Inc
Key facts
| Event ID | 73907 |
|---|---|
| Recall numbers | Z-1601-2016 |
| Recalling firm | Siemens Medical Solutions USA, Inc |
| Product type | Devices |
| Products | Syngo Dynamics; Kinetdx Picture Archiving and Communications System |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Siemens has identified changes in default carry forward workflow using VA10B_HF03 version of Syngo Dynamics. If the template design has measurements inside a carry forward-configured report section… |
| Initiation date | Apr 14, 2016 |
| Report date | May 11, 2016 |
| Termination date | Mar 20, 2017 |
| City | Malvern |
| State | PA |
| Country | United States |
| FEI number | 2240869 |
At a glance
- 1–9 Products in this recall
- None 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: