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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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Spectra Optia Apheresis System, REF: 61000, Caridian BCT, Lakewood, CO 80215. A blood component s... | 2 | 11/16/2011 | Caridian BCT, Incorporated |
| Spectra Optia Apheresis System, REF: 61000, CaridianBCT, Lakewood, CO 80215. The Spectra Optia Ap... | 2 | 06/28/2011 | Caridian BCT, Incorporated |
| Terumo BCT Lakewood, CO 80215, Catalog No 61000 Spectra Optia Apheresis System, Country of Origin: U... | 2 | 05/30/2012 | CaridianBCT, Inc. |
| Caridian BCT COBE Spectra System Blood Warmer, Catalog number 950000000. | 2 | 05/09/2012 | CaridianBCT, Inc. |
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