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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K141458
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Product Description
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FDA Recall
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MOL2150 Simplexa HSV 1&2 Direct -CSF -Genital Swab -Cutaneous / Mucocutaneous Swabs Product Usage: i... 2 07/10/2020 DiaSorin Molecular LLC
Simplexa HSV 1&2 Direct (MOL2150) with Direct Amplification Disc (MOL1451, MOL1452, MOL1455) Mode... 1 04/02/2016 Focus Diagnostics Inc
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