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CAREFUSION

10 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
BD MaxGuard Extension Set with 4-way stopcock, REF: M4058 recall (Z-1752-2022)CAREFUSION2022-09-13
BD MaxGuard Extension Set, REF: ME1069 recall (Z-1753-2022)CAREFUSION2022-09-13
BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS106 recall (Z-1754-2022)CAREFUSION2022-09-13
BD MaxGuard Flow Controller Extension Set with Needleless Y-Site, REF: MFS141 recall (Z-1755-2022)CAREFUSION2022-09-13
BD MaxGuard Drop Administration set with 3 Needleless Y-Sites Removable 3-port Manifold an recall (Z-1756-2022)CAREFUSION2022-09-13
BD MaxGuard Extension Set with 2 Needleless Y-Site, REF: MX9059 recall (Z-1757-2022)CAREFUSION2022-09-13
BD MaxGuard Extension Set with 0.2 Micron Filter and Needleless Y-Site, REF: MX9166 recall (Z-1758-2022)CAREFUSION2022-09-13
BD MaxGuard Extension Set with 1.2 Micron Filter and Needleless Y-Site, REF: MX9171 recall (Z-1759-2022)CAREFUSION2022-09-13
BD MaxGuard 15 Drop Administration Set with 4 Needleless Y-Sites, REF: MX9433 recall (Z-1760-2022)CAREFUSION2022-09-13
NicoletOne vEEG System, VIASYS Healthcare, Inc., Madison, Wisconsin 53711. recall (Z-1256-2010)CareFusion2010-04-07

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Every clearance here is in the API, with alerts when new ones post.