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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-0588-2016
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Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter, 9 Fr. Model 8104, 8105, 8106, 8107, 810... 2 01/05/2016 FEI # 2124215
Boston Scientific Corporation
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