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U.S. Department of Health and Human Services

Medical Device Recalls

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1 result found
510(K) Number: K895770
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Product Description
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Recall
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FDA Recall
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Recalling Firm
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Exel Huber Infusion Set (Catalog Numbers 26940R, 26941R, 26944R, 26945R, 26946R, 26948R, 26949R, 269... 1 01/22/2010 Exelint International Co.
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