Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K822210 |
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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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804115, Terumo Coronary Ostia cannula, 10 Fr, 10 (25 cm) long A cardiopulmonary bypass vascular ... | 1 | 06/14/2011 | Terumo Cardiovascular Systems Corporation |
804117, Terumo Coronary Ostia cannula, 12 Fr, 10 (25 cm) long A cardiopulmonary bypass vascular ... | 1 | 06/14/2011 | Terumo Cardiovascular Systems Corporation |
804159, Terumo Coronary Ostia cannula, 14 Fr, 10 (25 cm) long A cardiopulmonary bypass vascular ... | 1 | 06/14/2011 | Terumo Cardiovascular Systems Corporation |
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