Medical Device Recalls
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1 result found
Recall Date to: 04/11/2014 510(K) Number: K090971 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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BD ProbeTec Neisseria gonorrhoeae (GC) Qx Amplified DNA Assay Reagent Pack, REF 441124, contains 12 ... | 2 | 05/03/2013 | Becton Dickinson & Co. |
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