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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-2023-2025
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BD BACTEC MGIT 960 PZA Kit. IVD qualitative procedure for susceptibility testing of Mycobacterium tu... 2 06/25/2025 FEI # 1119779
Becton Dickinson & Co.
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