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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 15 of 15 Results
Related Medical Device Recalls
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Z-1762-2024 - DURAFLOW 2, 32CM STRAIGHT BASIC KIT PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012035 2 05/03/2024 FEI # 1319211
Angiodynamics, Inc.
Z-1765-2024 - DURAFLOW 2, 28CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012195 2 05/03/2024 FEI # 1319211
Angiodynamics, Inc.
Z-1761-2024 - DURAFLOW 2, 28CM STRAIGHT BASIC KIT, 1 per Bx PG-Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012021 2 05/03/2024 FEI # 1319211
Angiodynamics, Inc.
Z-1764-2024 - DURAFLOW 2, 24CM STRAIGHT VASC-PAK PG- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H787103012185 2 05/03/2024 FEI # 1319211
Angiodynamics, Inc.
Z-1774-2024 - BioFlo DuraMax 15.5F 24cm Single Valve Sheath VascPak Kit- Indicated for use in attaining Long-Term vascular access for Hemodialysis and Apheresis. Product Number: H965103038181 2 05/03/2024 FEI # 1319211
Angiodynamics, Inc.
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