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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Recalling Firm
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Z-1559-2008 - BD DifcoTM Neisseria Meningitidis Antisera Group Y, 228811, 1mL, in vials, which were labeled in part, 8019456 6250890 N. MEN. GP Y UNLABELED LYOPH, Becton Dickinson and Company, Sparks, MD 21152. Th... 3 08/08/2008 BD Diagnostic Systems / Lee Laboratories
Z-1562-2008 - BD DifcoTM Neisseria Meningitidis Antiserum Group Y 241113, 1mL, in vials, which were labeled in part, 8019456 6250890 N. MEN. GP Y UNLABELED LYOPH, Becton, Dickinson and Company, Sparks, MD 21152. Th... 3 08/08/2008 BD Diagnostic Systems / Lee Laboratories
Z-1561-2008 - BD DifcoTM Neisseria Meningitidis Antisera Group Y 241113, 1mL, in vials, which were labeled in part, 8019456 6250890 N. MEN. GP Y UNLABELED LYOPH, Becton, Dickinson and Company, Sparks, MD 21152. The... 3 08/08/2008 BD Diagnostic Systems / Lee Laboratories
Z-1560-2008 - BD DifcoTM Neisseria Meningitidis Antisera Group Y 228811, 1mL, in vials, which were labeled in part, 8019456 6250890 N. MEN. GP Y UNLABELED LYOPH, Becton, Dickinson and Company, Sparks, MD 21152. The... 3 08/08/2008 BD Diagnostic Systems / Lee Laboratories
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