Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K131331 |
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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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| BD Phoenix M50 Instrument, labeled as the following: 1. BD Phoenix M50 Automated Microbiology Sys... | 2 | 10/23/2025 | Becton Dickinson & Co. |
| BD Phoenix M50 Automated Microbiology System Version or Model: 443624 Catalog Number: 443624 | 2 | 12/03/2024 | Becton Dickinson & Co. |
| BD Phoenix M50 instrument -Intended for the rapid identification (ID) and antimicrobial susceptibili... | 2 | 09/24/2024 | Becton Dickinson & Co. |
| BD Phoenix 100-Intended for the rapid identification (ID) and antimicrobial susceptibility testing (... | 2 | 09/24/2024 | Becton Dickinson & Co. |
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