Microsoft Amalga Unified Intelligence System (UIS), This is a software-only device, WHIE Implementation v1.1i. A calculator/data processing module, for clinical use. Intended to provide the clinical user with the ability to view data from multiple, different data systems.
FDA Recall Z-0507-2012 · Posted 2012-01-11
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Recalling FirmMicrosoft Corporation Health Solutions Group
Recall StatusTerminated
Product CodeJQP
Date Initiated2010-07-27
Date Terminated2011-12-20
Product Quantity1
Reason for Recall
The database may incorrectly match patient data resulting in the incorrect patient data being displayed. This could potentially present a risk to patient safety.
Firm Action
Microsoft notified the sole consignee by FAX on 7/22/2010 with an Urgent Medical Device Safety Information. The letter identified the affected product, the description of the problem, and actions to be taken to correct the problem, along with some additional information for the consignee. In the interim, the firm proposes to block access to patient records identified as mismatched. The firm also stated that the issue has been addressed in version 2.0. The customer should report any incidents to Michael Stokes, Director of Policy Compliance at 208-938-5397 or via e-mail at [email protected].
Root Cause
Software design
Distribution Pattern
Nationwide Distribution -- Wisconsin.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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