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# 2 Covid-19 Product EUAs Revoked
- URL: https://www.fdaweb.com/2-covid-19-product-euas-revoked/
- Published: 2023-10-06T12:00:00.000Z
- Updated: 2026-09-14T19:01:17.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5155505

*Federal Register* notice: FDA is announcing the revocation of two Monkeypox-related Emergency Use Authorizations after the authorization holders requested they be revoked because the products are no longer being offered for sale. The affected products are Life Technologies’ TaqPath Monkeypox/Orthopox Virus DNA Kit, and Becton, Dickinson’s Viasure Monkeypox virus Real Time PCR Reagents for its BD MAX System. To view the notice, click [here](https://public-inspection.federalregister.gov/2023-22390.pdf?ref=fdaweb.com).