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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K180438
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FDA Recall
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BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings. Catalo... 2 02/09/2022 FEI # 1119779
Becton Dickinson & Co.
BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with the BD Veritor System Test Devic... 2 05/10/2019 FEI # 1119779
Becton Dickinson & Co.
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