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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
Recall Date to: 09/16/2014 PMA Number: P050048
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FSE Image Upgrade Kit, Catalog # 92019C This kit is used to install and/or upgrade software used ... 3 10/21/2013 Bio-Rad Laboratories
The Bio-Rad MONOLISA Anti-HBs EIA is for In Vitro Diagnostic Use and it has the catalog number 25220... 2 09/17/2012 Bio-Rad Laboratories
Bio-Rad's Monolisa (TM) Anti-HBs EIA test kit, Labeled as, "MONOLISA TM Anti-HBs EIA 25220; MONOL... 3 05/20/2010 Bio-Rad Laboratories
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