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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 38 Results
Related Medical Device Recalls
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Product Description
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Z-2198-2018 - BioFlo Midline 5F DL-20cm Max Sterile Barrier Drape Kit w/ Two Nitinol Guidewire PG, Catalog Number 46-490 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2199-2018 - BioFlo Midline 5F DL-20cm MST-45 Kit w/ Two Nitinol Guidewires PG, Catalog Number 46-810 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2200-2018 - RS TANDEM 5F DL XPP, Catalog Number 60M019881 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2201-2018 - RS 5F DL XPP, Catalog Number 60M030393 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2202-2018 - RS - TANDEM 5F DL BIOFLO MIDLINE, Catalog Number 60M035472 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2203-2018 - RS 5F DL BIOFLO PICC, Catalog Number 60M071831 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2204-2018 - RS TANDEM 5F DL BIOFLO PASV, Catalog Number 60M120196 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2205-2018 - RS 5F DL BIOFLO PASV, Catalog Number 60M132324 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2206-2018 - TANDEM 5F DL BIOFLO PASV, Catalog Number 60M140567 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
Z-2207-2018 - 5F DL BIOFLO PASV, Catalog Number 60M141006 2 06/14/2018 Angiodynamics Inc. (Navilyst Medical Inc.)
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