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Sunquest Information Systems, Inc. recalls Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
Recalled September 5, 2012 · FDA recall Z-2270-2012 · Sunquest Information Systems
Hazard
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory versions 6.4 and later while using Microbiology Result Entry (MRE), the specimen ribbon containing the Accession Number (AN) and the Battery Name may be missing or contain the wrong information. · FDA Class II
Units
127 sites
Sold at
Worldwide Distribution -- USA (nationwide) and the country of Canada.
Description
The recall was initiated because Sunquest has confirmed that the Sunquest Laboratory versions 6.4 and later while using Microbiology Result Entry (MRE), the specimen ribbon containing the Accession Number (AN) and the Battery Name may be missing or contain the wrong information.
Product
Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
Manufacturer(s)
Sunquest Information Systems, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →