Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K023870 |
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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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Boston Scientific (1) Flexima Regular Biliary Catheter System with RO Marker, 8 FR (2.7 mm) with ... | 2 | 08/27/2009 | Boston Scientific Corporation |
Boston Scientific, Flexima® and Percuflex® Drainage Catheter Family (Pigtail Style) ... | 2 | 05/21/2009 | Boston Scientific Corporation |
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