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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 13 Results
510(K) Number: K110901
 
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Product Description
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FDA Recall
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Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospi... 1 10/19/2012 Hospira Inc.
Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Hospi... 1 10/19/2012 Hospira Inc.
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List... 2 11/04/2016 Hospira Inc.
Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids. List... 2 11/04/2016 Hospira Inc.
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Produ... 2 11/03/2016 Hospira Inc.
Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids; Produ... 2 11/03/2016 Hospira Inc.
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Dev... 2 10/24/2016 Hospira Inc.
Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Devic... 2 10/24/2016 Hospira Inc.
Symbiq Two Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Devic... 2 06/27/2016 Hospira Inc.
Symbiq One Channel Infuser; an Rx medical device infusion pump used to administer I.V. fluids Devic... 2 06/27/2016 Hospira Inc.
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