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U.S. Department of Health and Human Services

Medical Device Recalls
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Z-0836-2022 - Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog Number 610210 GenePOC branded Revogene: Catalog Number 130840 2 03/30/2022 Meridian Bioscience Inc
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