Device recall
Z-1082-2012: Microsoft Amalga - previously known as Microsoft Amalga Unified Intelligence…
FDA device recall · Class II · Microsoft Corporation Health Solutions Group
Key facts
| Recall number (Z-number) | Z-1082-2012 |
|---|---|
| Recall event | 60890 |
| Product | Microsoft Amalga - previously known as Microsoft Amalga Unified Intelligence System (UIS) 2009 Product Usage: Microsoft Amalga UIS 2009 enables healthcare providers to create a comprehensive continually updated data ecosystem to aggregate, store, display, and share disparate data either coming from… |
| Product code | JQP |
| Recalling firm | Microsoft Corporation Health Solutions Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 12, 2012 |
| FEI number | 3007734659 |
At a glance
- None 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