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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-0004-2022 - Alinity m SARS-CoV-2 Amp Kit (Emergency Use Authorization, US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic 1 10/14/2021 FEI # 3005248192
Abbott Molecular, Inc.
Z-0005-2022 - Alinity m Resp-4-Plex AMP Kit (Emergency Use Authorization, US Assay) and Alinity m Resp-4-Plex Application Specification File. in vitro diagnostic 1 10/14/2021 FEI # 3005248192
Abbott Molecular, Inc.
Z-0008-2022 - Alinity m Resp-4-Plex AMP Kit (Non-US Assay) and Alinity m Resp-4-Plex Application Specification File. in vitro diagnostic 1 10/14/2021 FEI # 3005248192
Abbott Molecular, Inc.
Z-0007-2022 - Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic 1 10/14/2021 FEI # 3005248192
Abbott Molecular, Inc.
Z-0006-2022 - Alinity m SARS-CoV-2 Amp Kit (Non-US Assay) and Alinity m SARS-CoV-2 Application Specification File. in vitro diagnostic 1 10/14/2021 FEI # 3005248192
Abbott Molecular, Inc.
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