Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K811378 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Boston Scientific vanSonnenberg Sump with ''J'' Tip, 30 cm, 14Fr (4.7 mm), for percutaneous abscess ... | 2 | 09/13/2006 |
FEI # 1828132 Boston Scientific Corp |
| Malecot Nephrostomy Catheter System, Product Number: M001224110, GTIN: 08714729030980 The Maleco... | 2 | 03/18/2018 |
FEI # 3005099803 Boston Scientific Corporation |
| Boston Scientific, Flexima® and Percuflex® Drainage Catheter Family (Pigtail Style) ... | 2 | 05/21/2009 |
FEI # 3002095335 Boston Scientific Corporation |
| Boston Scientific, Flexima® and Percuflex® Drainage Catheter Family (Pigtail Style) ... | 2 | 05/21/2009 |
FEI # 3002095335 Boston Scientific Corporation |
| Boston Scientific, Flexima® and Percuflex® Drainage Catheter Family (Pigtail Style) ... | 2 | 05/21/2009 |
FEI # 3002095335 Boston Scientific Corporation |
| Boston Scientific, Flexima® and Percuflex® Drainage Catheter Family (Pigtail Style) ... | 2 | 05/21/2009 |
FEI # 3002095335 Boston Scientific Corporation |
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