Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K922475 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BD BACTEC Blood Culture System, labeled as the following: 1. BACTEC 9120 System, Catalog Numbers:... | 2 | 10/23/2025 | Becton Dickinson & Co. |
| BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 | 2 | 12/03/2024 | Becton Dickinson & Co. |
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