Medical Device Recalls
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1 result found
510(K) Number: K162443 |
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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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PowerPICC Provena Catheters, as 3 Fr. Single lumen and 4 Fr. Dual Lumen. Packaged in a poly tray wi... | 2 | 02/06/2018 | Bard Access Systems Inc. |
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