Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K180438 |
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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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BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalo... | 2 | 02/09/2022 | Becton Dickinson & Co. |
BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devic... | 2 | 05/10/2019 | Becton Dickinson & Co. |
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