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Sunquest Information Systems, Inc. recalls Sunquest Laboratory LabAccess Results Workstation (LARS)
Recalled September 5, 2012 · FDA recall Z-2272-2012 · Sunquest Information Systems
Hazard
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results. · FDA Class II
Units
151 sites
Sold at
Worldwide Distribution, including Nationwide (USA) and the countries of Canada, Denmark, Ireland, the United Arab Emirates and the United Kingdom.
Description
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory LabAccess Results Workstation (LARS) may file results to the wrong patient by incorrectly combining results.
Product
Sunquest Laboratory LabAccess Results Workstation (LARS)
Manufacturer(s)
Sunquest Information Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →