Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K974883 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube, part # 245122, packaged in 100 ct cartons and... | 2 | 10/19/2013 |
FEI # 1119779 Becton Dickinson & Co. |
| BD BACTEC(tm) MGI (tm) System Software, Catalog 445922, Lot V5.02A. Product Usage: The BACTEC(t... | 2 | 07/28/2011 |
FEI # 1119779 Becton Dickinson & Co. |
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