Medical Device Recalls
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1 result found
510(K) Number: K003100 |
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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, WALLGRAFT®® OVER-THE-WIRE, Tracheobronchial Endoprosthesis, Made in IRELAND, Ball... | 2 | 07/15/2011 | Boston Scientific Corporation |
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