Medical Device Recalls
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1 result found
510(K) Number: K181324 |
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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 plus (Pneumoplus) Part Numbers: Part No: RFIT-ASY-0143 / UDI: 00815381... | 2 | 07/08/2021 | BioFire Diagnostics, LLC |
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