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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 6 of 6 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-2380-2016 - Brilliance 64 CT Model 728231; To produce cross-sectional images of the body. 2 08/10/2016 Philips Medical Systems (Cleveland) Inc
Z-2381-2016 - Brilliance iCT, Model No. 728306; To produce cross-sectional images of the body. 2 08/10/2016 Philips Medical Systems (Cleveland) Inc
Z-2385-2016 - Ingenuity CT Model No. 728326; To produce cross-sectional images of the body. 2 08/10/2016 Philips Medical Systems (Cleveland) Inc
Z-2383-2016 - Ingenuity Core Model No. 728321; To produce cross-sectional images of the body. 2 08/10/2016 Philips Medical Systems (Cleveland) Inc
Z-2384-2016 - Ingenuity Core128 Model No. 728323; To produce cross-sectional images of the body. 2 08/10/2016 Philips Medical Systems (Cleveland) Inc
Z-2382-2016 - Brilliance iCT SP Model No. 728311; To produce cross-sectional images of the body. 2 08/10/2016 Philips Medical Systems (Cleveland) Inc
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