Medical Device Recalls
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1 result found
Recall Number: Z-0715-2016 |
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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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| Allura CV20; Model Number: 722031 The Allura CV2O is intended for physicians (e.g. cardiologists ... | 2 | 01/30/2016 |
FEI # 1218950 Philips Electronics North America Corporation |
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