06/26/2020 12:00 AM EDT
Source: U.S. Food and Drug Administration (FDA). Published: 6/26/2020. This three-page fact sheet informs healthcare providers of the significant known and potential risks and benefits of the emergency use of Access SARS-CoV-2 IgG. Access SARS-CoV-2 IgG is authorized for the detection of IgG antibodies to SARS-CoV-2 in human serum, serum separator tubes, and plasma (lithium heparin, dipotassium EDTA, tripotassium EDTA, sodium citrate). (PDF)
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