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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Related Medical Device Recalls Recall Date to: 10/01/2014
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Product Description
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Class
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FDA Recall
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Z-1690-2012 - Brilliance 16 - Model #728246, CT Scanning System is subject to recall/correction Product Usage: The Brilliance 6, 16, 40 64, Big Bore, iCT, iCT SP and Ingenuity CT are Computed Tomography X-Ray S... 2 05/30/2012 Philips Medical Systems (Cleveland) Inc
Z-1693-2012 - Brilliance iCT - Model #728306, and Brilliance iCT SP - Model #728311, CT Scanning System is subject to recall/correction Product Usage: The Brilliance 6, 16, 40 64, Brilliance Big Bore, iCT, iC... 2 05/30/2012 Philips Medical Systems (Cleveland) Inc
Z-1692-2012 - Brilliance Big Bore - Model #728243, and - Model #728244, CT Scanning System is subject to recall/correction Product Usage: The Brilliance 6, 16, 40 64, Brilliance Big Bore, iCT, iCT SP and In... 2 05/30/2012 Philips Medical Systems (Cleveland) Inc
Z-1691-2012 - Brilliance 40 - Model #72835, and Brilliance 64 - Model #728231, and Ingenuity - Model #728326, CT Scanning Systems are subject to recall/correction Product Usage: The Brilliance 6, 16, 40 64, ... 2 05/30/2012 Philips Medical Systems (Cleveland) Inc
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