Medical Device Recalls
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1 result found
510(K) Number: K212727 |
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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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FilmArray Pneumonia Panel (Pneumo), REF: RFIT-ASY-0145, For FILMARRAY systems, CE 2797, IVD, Rx Only | 2 | 08/21/2023 | BioFire Diagnostics, LLC |
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