FDA Medical Device Recalls (openFDA)
Microsoft Corporation Health Solutions Group: 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 many source systems or directly entered by end users for rapid self-service data exploration and analysis by front line managers, clinicians and ancillary staff. Furthermore, Amalga UIS allows healthcare providers to rapidly create new applications to respond to evolving business and clinical needs.
- Recall number
- Z-1082-2012
- Recalling firm
- Microsoft Corporation Health Solutions Group
- 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 many source systems or directly entered by end users for rapid self-service data exploration and analysis by front line managers, clinicians and ancillary staff. Furthermore, Amalga UIS allows healthcare providers to rapidly create new applications to respond to evolving business and clinical needs.
- Status
- Terminated
- Initiated
- 2012-01-04
- Posted
- 2012-02-22
- Terminated
- 2012-12-12
- Reason
- 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.
- Root cause
- Software design
- Action
- 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.
- Quantity
- 9 units
- Distribution
- Worldwide Distribution - USA (nationwide) including the states of California, China, Kentucky, North Carolina, Wisconsin and country of Switzerland.
- Lot, serial or model codes
- Software Version: R2 SP2, RTM, R2 SP3
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- JQP
- Firm FEI
- 3007734659
- Firm city
- Redmond
- Firm state
- WA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28