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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K882594
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Product Description
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FDA Recall
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ColorGard, latex-free, Midlength Secondary I.V. Set, convertible pin, 40 inch with Orange striped tu... 2 04/15/2010 Hospira Inc.
ColorGard, latex-free, Midlength Secondary I.V. Set, convertible pin, 40 inch with Purple striped tu... 2 04/15/2010 Hospira Inc.
ColorGard, latex-free, Midlength Secondary I.V. Set, convertible pin, 40 inch with Green striped tub... 2 04/15/2010 Hospira Inc.
Omniflow 4000 Plus, List numbers 40051-04-05, 40051-04-07, 40051-04-09, 40051-04-51; AC cord manufac... 2 10/06/2009 Hospira Inc
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