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# EUA for Abbott’s BinaxNow Revoked
- URL: https://www.fdaweb.com/eua-for-abbotts-binaxnow-revoked/
- Published: 2022-03-18T12:00:00.000Z
- Updated: 2026-09-14T17:37:08.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5151399

*Federal Register* notice: FDA has revoked an Emergency Use Authorization (EUA) issued to Abbott Diagnostics Scarborough for the BinaxNOW Covid-19 Ag Card 2 Home Test. FDA says Abbott never marketed the test under the EUA, and the product is subsequently marketed and covered by a subsequent EUA. To view the notice, click [here](https://public-inspection.federalregister.gov/2022-05892.pdf?ref=fdaweb.com).