Medical Device Recalls
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1 to 5 of 5 Results
Related Medical Device Recalls |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-1378-2012 - CDI Blood Parameter Monitoring System 500, 500AVHCT. Intended for use during cardiopulmonary bypass procedures. | 2 | 04/06/2012 | Terumo Cardiovascular Systems Corporation |
Z-1379-2012 - CDI Blood Parameter Monitoring System 500, 500AHCT. Intended for use during cardiopulmonary bypass procedures. | 2 | 04/06/2012 | Terumo Cardiovascular Systems Corporation |
Z-1382-2012 - CDI Blood Parameter Monitoring System 500, 500V. Intended for use during cardiopulmonary bypass procedures. | 2 | 04/06/2012 | Terumo Cardiovascular Systems Corporation |
Z-1381-2012 - CDI Blood Parameter Monitoring System 500, 500A. Intended for use during cardiopulmonary bypass procedures. | 2 | 04/06/2012 | Terumo Cardiovascular Systems Corporation |
Z-1380-2012 - CDI Blood Parameter Monitoring System 500, 500AV. Intended for use during cardiopulmonary bypass procedures. | 2 | 04/06/2012 | Terumo Cardiovascular Systems Corporation |
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