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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-0720-2016
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INTEGRIS BH3000; Model Number: 72242 The Philips INTEGRIS 3000 I 5000 system is intended for inte... 2 01/30/2016 FEI # 1218950
Philips Electronics North America Corporation
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