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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 21 Results
510(K) Number: K031538
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Product Description
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FDA Recall
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Boston Scientific EndoVive 24F (8 mm) Safety PEG Kit, Push Method for use with sterile Xylocaine amp... 2 06/25/2015 Boston Scientific Corp
Boston Scientific EndoVive 20Fr (6.7 mm) Safety PEG Kit, Push Method, latex free, sterile, Boston Sc... 2 01/28/2009 Boston Scientific Corp
Boston Scientific EndoVive 20F (6.7 mm) Safety PEG Kit, Push Method for use with sterile Xylocaine a... 2 01/28/2009 Boston Scientific Corp
Boston Scientific EndoVive 24F (8 mm) Safety PEG Kit, Push Method for use with sterile Xylocaine amp... 2 01/28/2009 Boston Scientific Corp
Boston Scientific EndoVive 20F (6.7 mm) Safety PEG Kit, Push Method for use with pre-filled lidocain... 2 01/28/2009 Boston Scientific Corp
Boston Scientific brand Standard PEG (percutaneous endoscopic gastrostomy tubes) Kit, 24 Fr, push; ... 2 07/07/2005 Boston Scientific Corp
Boston Scientific brand pull Gastro-dome (percutaneous endoscopic gastrostomy tubes) Kit, 24 Frl; ca... 2 07/07/2005 Boston Scientific Corp
Boston Scientific brand pull Gastro-dome (percutaneous endoscopic gastrostomy tubes) Kit, 20 Frl; ca... 2 07/07/2005 Boston Scientific Corp
Boston Scientific brand Standard PEG (percutaneous endoscopic gastrostomy tubes) Kit, 24 Fr, pull; ... 2 07/07/2005 Boston Scientific Corp
Boston Scientific brand Standard PEG (percutaneous endoscopic gastrostomy tubes) Kit, 20 Fr, push; ... 2 07/07/2005 Boston Scientific Corp
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