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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
Related Medical Device Recalls Date Classified to: 10/21/2014
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Product Description
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Recall
Class
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Date
Posted
Sort by Date Classified [0-9]
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Recalling Firm
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Z-0676-2007 - OEC 9900 Elite image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0677-2007 - OEC 9800 image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0678-2007 - OEC 8800 image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0683-2007 - OEC 9900 Elite (NAV) Image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0680-2007 - OEC FluoroTrak 9800 PLUS, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0681-2007 - OEC 9800 MD Motorized C-Arm System, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0682-2007 - OEC 9800 Plus (Fluorotrak), Image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
Z-0679-2007 - OEC 9900 Elite MD Motorized C-Arm System, image-intensified fluoroscopic x-ray system, GE Healthcare, Salt Lake City, UT. 2 Sep-28-2007 GE OEC Medical Systems, Inc
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