Labcorp receives emergency use authorization for first non-prescription at-home collection kit for combined COVID-19, flu and RSV detection
New Offering Enhances Portfolio of Leading COVID-19 PCR Testing Options
Combined Kit Provides People with Trusted Answers from the Comfort of
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The Pixel by Labcorp COVID-19+Flu+RSV Test Home Collection Kit will be available for use by individuals age 2 and older through the Labcorp OnDemand™ digital health platform without a prescription. For those who meet clinical guidelines and have insurance, the kit is available at no upfront cost. By using the
“Labcorp’s COVID-19 tests have been trusted by physicians and millions of people throughout the pandemic. This new at-home collection kit makes it easier for consumers to access testing for multiple respiratory viruses – COVID-19, the flu and RSV – that can present similar symptoms,” said Dr.
The Pixel by Labcorp COVID-19+Flu+RSV Test Home Collection Kit is shipped via FedEx Priority Overnight to an individual’s home. Once collected, the sample is returned to
If a person tests positive, they will receive a call from a third-party physician network with detailed next steps and access to a free clinician consult. Clinical guidelines for receiving the kit at no upfront cost with insurance include experiencing symptoms, being exposed to someone with COVID-19, or receiving a request to get tested from a health care provider. This test is only intended for individuals experiencing flu-like symptoms.
The new at-home test collection kit is the latest example of Labcorp’s commitment to delivering innovations that help physicians, health systems and consumers respond to the pandemic.
Labcorp’s combined home collection kit for COVID-19, influenza A/B and RSV has not been FDA cleared or approved and has been authorized by the FDA under an emergency use authorization only for the detection of nucleic acid from SARS-CoV-2, influenza A and/or influenza B, and RSV, not for any other viruses or pathogens. The test is only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of in vitro diagnostic tests for detection and/or diagnosis of COVID-19 under Section 564(b)(1) of the Act, 21 U.S.C. § 360bbb-3(b)(1), unless the authorization is terminated or revoked sooner.
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