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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-1014-2024
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BD BBL Sensi Disc Augmentin - 3¿g, Catalog Number 291270¿used for semi-quantitative in vitro suscept... 2 02/08/2024 FEI # 1119779
Becton Dickinson & Co.
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