Medical Device Recalls
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1 result found
Recall Number: Z-2114-2016 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Ingenuity Core 128, model #728323; Intended to produce cross- sectional images of the body. | 2 | 06/30/2016 |
FEI # 1525965 Philips Medical Systems (Cleveland) Inc |
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