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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K881321
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Product Description
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Y-Type Blood/Solution Set, catalog #1C8459; Standard Blood Filter (170 to 260 micron), Drip Chamber ... 2 01/16/2003 FEI # 1416980
Baxter Healthcare Corp.
Y-Type Blood/Solution Set, catalog #1C8117; Standard Blood Filter (170 to 260 micron), Drip Chamber ... 2 01/16/2003 FEI # 1416980
Baxter Healthcare Corp.
Y-Type Blood/Solution Set, catalog #1C8029; Standard Blood Filter (170 to 260 micron), Drip Chamber ... 2 01/16/2003 FEI # 1416980
Baxter Healthcare Corp.
Y-Type Blood/Solution Set with Pressure Pump, catalog #1C8658; Standard Blood Filter (170 to 260 mic... 2 01/16/2003 FEI # 1416980
Baxter Healthcare Corp.
Interlink Y-Type Blood/Solution Set with Standard Bore 4-way Stopcock Extension Set, catalog #3C0116... 2 01/16/2003 FEI # 1416980
Baxter Healthcare Corp.
Fenwal Y-Type Blood Component Recipient Set with Standard Blood Filter, 10 drops/mL, 65'', 170 to 26... 2 08/21/2003 FEI # 1416980
Baxter Healthcare Corp.
Fenwal Blood Component Recipient Set with Standard Blood Filter, 10 drops/mL, 55'', 170 to 260 Micro... 2 08/21/2003 FEI # 1416980
Baxter Healthcare Corp.
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