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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: K033244
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Product Description
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FDA Recall
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GE Healthcare, Innova 2100IQ, Innova 3100, Innova 3100IQ, Innova 4100, Innova 4100IQ Innova 2121IQ, ... 2 03/10/2014 GE Healthcare, LLC
GE Healthcare, Innova 3100 and Innova 4100 systems. The Digital Fluoroscopic Imaging System is in... 2 06/28/2013 GE Healthcare, LLC
GE Healthcare, Innova 2100IQ, Innova 3100IQ, Innova 4100IQ, Cardiovascular and Interventional Im... 2 04/18/2013 GE Healthcare, LLC
GE Healthcare Advantx, Innova2000, Innova3100, Innova4100, Innova2100IQ, Innova3100IQ, and Innova41... 2 03/13/2013 GE Healthcare, LLC
Innova 3100/ 3100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopi... 2 06/29/2010 Ge Healthcare, Llc
Innova 2100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopic imag... 2 06/29/2010 Ge Healthcare, Llc
Innova 4100/4100IQ system with InnovaIQ Table Option Indicated for use in generating fluoroscopi... 2 06/29/2010 Ge Healthcare, Llc
GE Healthcare, GE Innova 4100 / 4100 IQ. , ( The system consists of an a monoplane positioner, a va... 2 11/09/2009 GE Medical Systems, LLC
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