Medical Device Recalls
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1 result found
510(K) Number: K003006 |
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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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Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes | 2 | 09/30/2015 | Arrow International Inc |
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