Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K926018 |
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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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BBL CrystaLEAD Enteric/Nonfermentor (E/NF) Identification (ID) System, catalog number 245000. in v... | 3 | 07/11/2014 | Becton Dickinson & Co. |
Becton, Dickinson and Company, BBL Crystal Enteric/Nonfermenter ID Kit, Catalog # 24500, cartons of ... | 2 | 01/20/2013 | Becton Dickinson & Co. |
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