Medical Device Recalls
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1 to 10 of 38 Results
Related Medical Device Recalls |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Z-2207-2018 - 5F DL BIOFLO PASV, Catalog Number 60M141006 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2210-2018 - 5F DL BIOFLO PICC, Catalog Number 60M180592 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2191-2018 - Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved PG, Catalog Number 45-872 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2194-2018 - Bio-Stable 5F DL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-887 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2190-2018 - Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved PG, Catalog Number 45-871 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2196-2018 - Bio-Stable 5F DL-55CM MST-70 KIT Non-Valved with Nitinol Guidewire PG, Catalog Number 45-895 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2193-2018 - Bio-Stable 5F SL-55CM IR-145 Kit Non-Valved with Nitinol GW PG, Catalog Number 45-886 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2189-2018 - Bio-Stable 5F SL-55CM IR-145 Kit Valved PG, Catalog Number 45-818 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2192-2018 - Bio-Stable 5F SL-55CM IR-145 Kit Valved with Nitinol GW PG, Catalog Number 45-882 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
Z-2195-2018 - Bio-Stable 5F SL-55CM MST-70 Kit Valved with Nitinol Guidewire PG, Catalog Number 45-892 | 2 | 06/14/2018 | Angiodynamics Inc. (Navilyst Medical Inc.) |
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