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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 17 Results
510(K) Number: K811078
 
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Product Description
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Baxter Y-Type Minivolume Extension Set; catalog 1C8499; Baxter Healthcare Corporation, Deerfield, IL... 1 02/06/2003 Baxter Healthcare Corp.
Baxter Auto Syringe Micro-Volume Extension Set with 0.22 Micron Filter, catalog 1M8516 and 1M8516Y; ... 1 02/06/2003 Baxter Healthcare Corp.
Baxter Auto Syringe Micro-Volume Extension Set with 0.22 Micron Filter, catalog 1M8522 and 1M8522Y; ... 1 02/06/2003 Baxter Healthcare Corp.
Baxter Auto Syringe Micro-Volume Extension Set with 0.22 Micron Filter, catalog 1M8527 and 1M8527Y; ... 1 02/06/2003 Baxter Healthcare Corp.
Baxter AutoSyringe Extension Set with 0.22 Micron Filter, catalog 1M8529; Baxter Healthcare Corporat... 1 02/06/2003 Baxter Healthcare Corp.
Baxter Minivolume T-Connector Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog... 1 02/06/2003 Baxter Healthcare Corp.
Baxter Minivolume Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2C5693; Bax... 1 02/06/2003 Baxter Healthcare Corp.
Baxter Interlink System Minivolume Extension Set, product code 1C8483; 18'', 1.3 mL Vol., with 0.22 ... 2 08/06/2005 Baxter Healthcare Corp.
Baxter Minivolume Extension Set, product code 2C5681; An Rx sterile, nonpyrogenic fluid pathway, 6.4... 2 03/24/2006 Baxter Healthcare Corp.
Baxter Y-Type Minivolume Extension Set, product code 1C8689; An Rx sterile, nonpyrogenic fluid pathw... 2 03/24/2006 Baxter Healthcare Corp.
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