Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K131694 |
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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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BioFlo Port with ENDEXO and PASV Technology-AngioDynamics BIOFLO 8F SINGLE PLASTIC NON-FILLED; VALVE... | 2 | 10/05/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Port Kit with Access Infusion Set under the following labels: 1) 8F/SL/Plastic Port/F, Product Numbe... | 2 | 01/24/2014 | Navilyst Medical, Inc. |
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