FDA-Device2012-09-05Class II
Sunquest Laboratory LabAccess Results Workstation (LARS)
Sunquest Information Systems, Inc.
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.
Sold states
Worldwide Distribution, including Nationwide (USA) and the countries of Canada, Denmark, Ireland, the United Arab Emirates and the United Kingdom.
Affected count
151 sites
Manufactured in
250 S Williams Blvd, N/A, Tucson, AZ, United States
Products
Sunquest Laboratory LabAccess Results Workstation (LARS)
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2272-2012Don't want to check this manually?
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