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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K103090
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Product Description
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FDA Recall
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Spectra Optia Apheresis System, REF: 61000, CaridianBCT, Lakewood, CO 80215. The Spectra Optia Ap... 2 06/28/2011 Caridian BCT, Incorporated
Spectra Optia Apheresis System, REF: 61000, Caridian BCT, Lakewood, CO 80215. A blood component s... 2 11/16/2011 Caridian BCT, Incorporated
Caridian BCT COBE Spectra System Blood Warmer, Catalog number 950000000. 2 05/09/2012 CaridianBCT, Inc.
Terumo BCT Lakewood, CO 80215, Catalog No 61000 Spectra Optia Apheresis System, Country of Origin: U... 2 05/30/2012 CaridianBCT, Inc.
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