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U.S. Department of Health and Human Services

Medical Device Recalls

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201 to 210 of 500 Results *
Recall Date to: 07/23/2014
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Product Description
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Class
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FDA Recall
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Recalling Firm
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Sunquest Laboratory SMART & Sunquest Laboratory SMART Select 3 08/16/2012 Sunquest Information Systems, Inc.
System 8000 Base Product Usage: The Sarns Modular Perfusion System 8000 is indicated for use fo... 3 08/16/2012 Terumo Cardiovascular Systems Corporation
TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Pa... 3 08/10/2012 Teleflex Medical
Dimension Vista(R) Vancomycin Flex(R) Reagent Cartridge (VANC, Catalog # K4086). For the quantita... 3 08/09/2012 Siemens Healthcare Diagnostics, Inc.
Cobas KRAS Mutation Test for In Vitro Diagnostic Use Product Usage: Usage: The Cobas KRAS Mutat... 3 08/08/2012 Roche Molecular Systems, Inc.
Model 731 EMV+ Uni-Vent, Impact Instrumentation Inc., 27 Fairfield Place, West Caldwell NJ 07006. In... 3 08/07/2012 Impact Instrumentation, Inc.
Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual recording of surgical ... 3 08/06/2012 Berchtold Corp.
IRISpec" CA/CB two-part urine chemistry control twin set, Iris Diagnostics part number 800-0074. ... 3 08/01/2012 Iris Diagnostics
SIGMASpectrum Infusion Pump Master Drug Library (MDL) Editor software. Product Usage: A custom... 3 07/18/2012 Sigma
Presage ST2 Assay, catalog numbers BC-1065 and BC-1065E. The Critical Diagnostics Presage ST2 Ass... 3 07/13/2012 Critical Diagnostics

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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