Microsoft Amalga - previously known as Microsoft Amalga Unified Intelligence System (UIS) 2009 Product Usage: Microsoft
FDA device recall Z-1082-2012 · posted 2012-02-22 · Terminated
Recall details
- Recalling firm
- Microsoft Corporation Health Solutions Group
- Reason for recall
- Healthcare providers reported that when sharing a single browser session on Amalga Web, patient A's data can be displayed under patient B's name.
- Action taken
- Microsoft Corporation sent an "Urgent Field Safety Notice" letter dated January 5, 2012 by email to all affected customers. The letter described the product, problem, and actions to be taken by the customers. If you have any questions about this corrective action program, please contact Microsoft Corporation at 425-882-8080.
- Root cause
- Software design
- Status
- Terminated
- Product code
- JQP
- Quantity affected
- 9 units
- Distribution
- Worldwide Distribution - USA (nationwide) including the states of California, China, Kentucky, North Carolina, Wisconsin and country of Switzerland.
- Date initiated
- 2012-01-04
- Date posted
- 2012-02-22
- Date terminated
- 2012-12-12
- Location
- Redmond, WA
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