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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: K083019
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Product Description
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FDA Recall
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The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the ... 1 11/21/2013 Hospira Inc.
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the ... 1 04/30/2013 Hospira Inc.
GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single chann... 1 04/26/2013 Hospira Inc.
GemStar Pump - Battery Product Usage: The GemStar Pump is a small and lightweight, single cha... 1 04/26/2013 Hospira Inc.
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the ... 2 04/15/2013 Hospira Inc.
The GemStar Pump is a small and lightweight, single channel infusion device designed for use in the ... 2 04/15/2013 Hospira Inc.
GemStar Bolus Cord; a remote bolus cord and switch for use with GemStar 7 Therapy and Pain Managemen... 2 04/26/2012 Hospira Inc.
GemStar SP Infusion Suite Database, Version 1.0; an Rx PC software application; Hospira, Inc., Lake ... 2 04/15/2011 Hospira Inc.
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