Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K032930 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Ultraflex Esophageal Stent System. Covered - Proximal Release - 18/23/12/9. Catalog Number M00513850... | 2 | 06/25/2010 | Boston Scientific Corporation |
Ultraflex Esophageal Stent System. Covered - Proximal Release - 18/23/15/12. Catalog Number M0051386... | 2 | 06/25/2010 | Boston Scientific Corporation |
Ultraflex Esophageal Stent System. Covered - Large - Distal Release - 23/28/10/7. Catalog Number M00... | 2 | 06/25/2010 | Boston Scientific Corporation |
Ultraflex Esophageal Stent System. Covered - Large - Distal Release - 23/28/12/9. Catalog Number M00... | 2 | 06/25/2010 | Boston Scientific Corporation |
Ultraflex Esophageal Stent System. Covered - Large - Proximal Release - 23/28/10/7. Catalog Number M... | 2 | 06/25/2010 | Boston Scientific Corporation |
Ultraflex Esophageal Stent System. Uncovered - Distal Release - 18/23/10. Catalog Number M00513710. ... | 2 | 06/25/2010 | Boston Scientific Corporation |
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