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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2111-2016 - Brilliance CT Big Bore Oncology, model #728243; Intended to produce cross- sectional images of the body. 2 06/30/2016 Philips Medical Systems (Cleveland) Inc
Z-2112-2016 - Brilliance iCT model #728306; Intended to produce cross- sectional images of the body. 2 06/30/2016 Philips Medical Systems (Cleveland) Inc
Z-2115-2016 - Ingenuity Core, model # 728326; Intended to produce cross- sectional images of the body. 2 06/30/2016 Philips Medical Systems (Cleveland) Inc
Z-2114-2016 - Ingenuity Core 128, model #728323; Intended to produce cross- sectional images of the body. 2 06/30/2016 Philips Medical Systems (Cleveland) Inc
Z-2113-2016 - Ingenuity Flex, model # 728317; Intended to produce cross- sectional images of the body. 2 06/30/2016 Philips Medical Systems (Cleveland) Inc
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