Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K121990 |
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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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| BioFlo PICC with ENDEXO and PASV, ( RS 5F DL BIOFLO PASV - MEMORIAL HOSPITAL SYSTEM (LTP) PG) Cat. ... | 2 | 12/11/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
| RS 5F DL XPP, Catalog Number 60M030393 | 2 | 06/14/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
| RS TANDEM 5F DL BIOFLO PICC, Catalog Number 60M250097 | 2 | 06/14/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
| RS TANDEM 5F DL XPP, Catalog Number 60M019881 | 2 | 06/14/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
| RS 5F DL XPP KIT, Catalog Number 60M183104 | 2 | 06/14/2018 |
FEI # 3017892510 Angiodynamics Inc. (Navilyst Medical Inc.) |
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