Medical Device Recalls
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1 result found
510(K) Number: K170158 |
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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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| PowerGlide ST Midline Catheter Maximal Barrier Kit-18 gauge,10 cm length Catalog Number: ST018101D | 2 | 05/09/2020 |
FEI # 2243072 Becton Dickinson & Company |
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