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Terminated

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.

FDA Recall Z-1082-2012 · Posted 2012-02-22

Recalling FirmMicrosoft Corporation Health Solutions Group
Recall StatusTerminated
Product CodeJQP
Date Initiated2012-01-04
Date Terminated2012-12-12
Product Quantity9 units

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.

Firm 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.

Root Cause

Software design

Distribution Pattern

Worldwide Distribution - USA (nationwide) including the states of California, China, Kentucky, North Carolina, Wisconsin and country of Switzerland.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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