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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
Related Medical Device Recalls Recall Date to: 08/21/2014
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Product Description
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FDA Recall
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Z-2125-2012 - OEC 9800 Plus Digital; MDL number A349855. Product Usage: Is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical and interventional procedures. Clini... 2 08/01/2012 GE OEC Medical Systems, Inc
Z-2127-2012 - UroView 2800; MDL number A349855. Product Usage: Designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical, and interventional procedures. Clinical applicat... 2 08/01/2012 GE OEC Medical Systems, Inc
Z-2126-2012 - OEC MiniView 6800 Mobile; MDL number A349855. Product Usage: The mini 6800 digital mobile c arm is designed to provide the physician with general fluoroscopic visualization of the patient includin... 2 08/01/2012 GE OEC Medical Systems, Inc
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