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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K171850
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Product Description
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FDA Recall
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Brilliance iCT (Model No. 728306), Software Version 4.1.6 Product Usage: Computed Tomography X-r... 2 10/31/2018 Philips Medical Systems (Cleveland) Inc
Brilliance 64 (Model No. 728231), Software version 4.1.6 Product Usage: Computed Tomography X-ra... 2 10/31/2018 Philips Medical Systems (Cleveland) Inc
Brilliance Big Bore Oncology CT (Model No. 728243) software version 4.2.0 Product Usage: Compute... 2 10/31/2018 Philips Medical Systems (Cleveland) Inc
IQon Spectral CT (Model No. 728332), Software Version 4.7.0 or 4.7.2 Product Usage: Computed Tom... 2 10/31/2018 Philips Medical Systems (Cleveland) Inc
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