Medical Device Recalls
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1 result found
510(K) Number: K060812 |
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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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BD Posiflush Saline Flush Syringe 10 ml inlcuded in the following device kits: PowerLoc Port Access ... | 2 | 03/13/2015 | Bard Access Systems |
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