Orders placed on Thursday, June 16 and Friday, June 17 will not ship until Monday June 20. We are sorry for the delay.
The Centers for Disease Control and Prevention (CDC)1 and the World Health Organization (WHO)2 have highlighted surveillance of the following Omicron lineages:
(1) BA.2.3.20, BA.2.75, BA.4.6, BA.5, BA.5.2.6, BF.7, BQ.1, BQ.1.1, and XBB
Additionally, six other variants have been under continued surveillance despite their lower prevalence:
(2) Delta (also known as B.1.617.2, all sublineages) first detected in India,
(3) Alpha (also known as B.1.1.7, all sublineages) first detected in the United Kingdom,
(4) Beta (also known as B.1.351, all sublineages) first detected in South Africa,
(5) Gamma (also known as P.1, all sublineages) first detected in Japan/Brazil,
(6) Lambda (also known as C.37, all sublineages) first detected in Peru,
(7) Mu (also known as B.1.621, all sublineages) first detected in Colombia
Lucira Health performs routine surveillance of emerging SARS-CoV-2 strains by periodically evaluating in silico reactivity against sequence databases. These evaluations have shown that these variants are reactive to the Lucira COVID-19 Check-It and All-In-One Test Kits. The Lucira Health assay targets two non-overlapping regions of the SARS-CoV-2 genome. The detection regions are unaffected by the mutations in the spike protein of SARS-CoV-2 in the variant strains.
Lucira Health will continue to monitor the situation with emerging variants of SARS-CoV-2.
If you have any questions on the above, please reach out to Technical Support at
techsupport@lucirahealth.com.
1 https://covid.cdc.gov/covid-data-tracker/#variant-proportions
2 https://www.who.int/en/activities/tracking-SARS-CoV-2-variants/
These home tests have not been FDA cleared or approved. These home tests have been authorized by FDA under Emergency Use Authorization (EUA). These home tests have been authorized only for the testing of nasal swabs for detection of nucleic acid from SARS-CoV-2 alone, or from SARS-CoV-2, influenza A, and influenza B; not for any other viruses or pathogens. These home tests are only authorized for the duration of the declaration that circumstances exist justifying the authorization of emergency use of IVDs 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 declaration is terminated or revoked sooner.
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