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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 8 of 8 Results
510(K) Number: K942024
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Product Description
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FDA Recall
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Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray cont... 2 10/24/2006 FEI # 2183502
Smiths Medical MD, Inc.
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray cont... 2 10/24/2006 FEI # 2183502
Smiths Medical MD, Inc.
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray cont... 2 10/24/2006 FEI # 2183502
Smiths Medical MD, Inc.
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... 2 04/27/2006 FEI # 2183502
Smiths Medical MD, Inc.
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... 2 04/27/2006 FEI # 2183502
Smiths Medical MD, Inc.
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... 2 04/27/2006 FEI # 2183502
Smiths Medical MD, Inc.
Locator-Wand Cover that is sold in a shelf carton (unit packaging) separate to the sterile tray con... 2 04/27/2006 FEI # 2183502
Smiths Medical MD, Inc.
Deltec branded PORT-A-CATH II Single-Lumen Low Profile Polysulfone/Titanium Venous Access System, Pr... 2 01/28/2005 FEI # 2183502
Smiths Medical MD, Inc.
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