Medical Device Recalls
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21 to 26 of 26 Results
510(K) Number: K972962 |
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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CDI Blood Parameter Monitoring System 500 Product Usage: The CDl Blood Parameter Monitoring Syst... | 2 | 01/11/2012 | Terumo Cardiovascular Systems Corporation |
CDI Blood Parameter Monitoring System 500 Product Usage: The CDl Blood Parameter Monitoring Syst... | 2 | 01/11/2012 | Terumo Cardiovascular Systems Corporation |
CDI Blood Parameter Monitoring System 500 Product Usage: The CDl Blood Parameter Monitoring Syst... | 2 | 01/11/2012 | Terumo Cardiovascular Systems Corporation |
CDI Blood Parameter Monitoring System 500 Product Usage: The CDl Blood Parameter Monitoring Syst... | 2 | 01/11/2012 | Terumo Cardiovascular Systems Corporation |
CDI Blood Parameter Monitoring System 500 with Venous Blood parameter module Catalog number 500... | 2 | 05/12/2011 | Terumo Cardiovascular Systems Corporation |
CDI Blood Parameter Monitoring System 500 with Arterial Blood parameter module Catalog number 50... | 2 | 05/12/2011 | Terumo Cardiovascular Systems Corporation |
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