Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K984631 |
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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" CT/GC/AC Reagent Pack, catalog #440450, labeled in part ***Becton Dickinson and Company... | 2 | 06/24/2011 | Becton Dickinson & Co. |
Becton Dickinson's ProbeTec (tm) ET Instrument | 1 | 08/20/2003 | Becton Dickinson & Co. |
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