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U.S. Department of Health and Human Services

Medical Device Recalls

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31 to 40 of 500 Results *
Recall Date to: 07/29/2015
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Product Description
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FDA Recall
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Device to determine quantitative total testosterone in human serum 2 11/06/2003 Qualigen Inc
Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, ... 3 02/07/2013 Diagnostic Hybrids Inc
Discovery ST PET/CT imaging system with gantry model number 5105797. Catalog Identifiers: S9114LA... 2 06/02/2006 General Electric Med Systems LLC
Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1: The Nidek Green La... 2 07/14/2015 Nidek Inc
Dual Tip Marker, Sterile Product Usage: A writing instrument intended to mark paper and pla... 3 03/29/2013 Viscot Medical LLC
ENT Pack - contains Devon Light Glove Used during surgery 2 07/07/2015 Stradis Healthcare, LLC.
Easypump L T 60-24 infusion pump 2 03/07/2006 I-Flow Corporation
Esprit Ventilator, Model V1000 manufactured with Power Supply PN 1015852 The Esprit Ventilator is... 2 09/17/2008 Respironics California Inc
Eye Pack - contains Devon Light Glove Used during surgery 2 07/07/2015 Stradis Healthcare, LLC.
Four Lead Arthroscopic Irrigation Set, for use with ARTHROMATIC Plastic Containers, Product Code 2C... 2 07/10/2013 Baxter Healthcare Corp.

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