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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
510(K) Number: K152842
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Product Description
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Recall
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FDA Recall
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Boston Scientific Wallstent Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding Sten... 2 09/13/2018 FEI # 3005057969
SPS Sterilization, Inc
Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 22MM X 45MM | 75CM... 2 09/13/2018 FEI # 3005057969
SPS Sterilization, Inc
Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Self-Expanding Stent, 10MM X 94MM | 1... 2 09/13/2018 FEI # 3005057969
SPS Sterilization, Inc
Boston Scientific Wallstent RP Endoprosthesis Tracheobronchial Transhepatic Biliary Self-Expanding S... 2 09/13/2018 FEI # 3005057969
SPS Sterilization, Inc
Boston Scientific Wallstent Endoprosthesis Tracheobronchial Self-Expanding Stent, 24MM X 70MM | 75CM... 2 09/13/2018 FEI # 3005057969
SPS Sterilization, Inc
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