Medical Device Recalls
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1 result found
510(K) Number: K070705 |
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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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| Bionector Needleless connector. Bionector is a multi-purpose catheter accessory; a closed needle-les... | 2 | 10/22/2014 |
FEI # 2245270 Vygon Corporation |
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