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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K931550
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Recall
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FDA Recall
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SmartSite Low Sorbing Infusion Set, Model#72313E The SmartSite Low Sorbing Infusion Sets are used... 2 09/26/2013 FEI # 2016493
CareFusion 303, Inc.
BD SE Burette Set 20 Drops 2 Injection Ports Vented/NonVented, REF: 72103E-0006 2 09/13/2021 FEI # 3012410077
CAREFUSION
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