Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K141458 |
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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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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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