FDA-Device2012-09-05Class II
Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
Sunquest Information Systems, Inc.
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.
Sold states
Worldwide Distribution -- USA (nationwide) and the country of Canada.
Affected count
127 sites
Manufactured in
250 S Williams Blvd, N/A, Tucson, AZ, United States
Products
Sunquest Laboratory Versions 6.4 and later using Microbiology Result Entry
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2270-2012Don't want to check this manually?
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