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U.S. Department of Health and Human Services

Medical Device Recalls

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111 to 120 of 500 Results *
Recall Date to: 09/15/2014
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Product Description
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FDA Recall
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Recalling Firm
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Life Force Chamber Product Usage:The product is intended for restful contemplation and spiritual... 2 09/11/2014 Life Force of Tampa, LLC
Hancock Apical Left Ventricle Connector, Model No. H174Axx, Catalog No. 0174ACP012. Used use in c... 2 09/11/2014 Medtronic Cardiovascular Surgery-the Heart Valve Division
Siemens Luminos dRF, Ysio or Uroskop Omnia systems. The Axiom Luminos dRF is intended to be used ... 2 09/10/2014 Siemens Medical Solutions USA, Inc
The BD MAX MRSA Assay, catalogue #442953. An automated qualitative in vitro diagnostic test for t... 2 09/10/2014 Becton Dickinson & Co.
Illumina Worklist Manager (IWM) (software v1.0.15), a component of Illumina MiSeqDx Platform. Pro... 2 09/09/2014 Illumina Inc
Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE, Rx only The Streamline MIS S... 2 09/09/2014 PIONEER SURGICAL TECHNOLOGY, INC.
***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m), 150 mL Burette***Drip Chamber Filter Val... 2 09/09/2014 Baxter Healthcare Corp
***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 In... 2 09/09/2014 Baxter Healthcare Corp
***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip Chamber Filter Valve***3 Lue... 2 09/09/2014 Baxter Healthcare Corp
Prime Care ® Transcend Mattress, Prime Care ® Transcend Perimeter Mattress, Prime Care ® Transcend A... 2 09/09/2014 Primus Medical LLC

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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