Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K030677 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Becton Dickinson Phoenix Update Disks (PUD), catalog # 441107/ 448047, component of BD automated mic... | 2 | 05/24/2012 |
FEI # 1119779 Becton Dickinson & Co. |
| Becton Dickinson Phoenix System Software, catalog # 448035/448046, component of BD automated microbi... | 2 | 05/24/2012 |
FEI # 1119779 Becton Dickinson & Co. |
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