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# FDA Revokes Roche Emergency Use Authorization on Zika Test
- URL: https://www.fdaweb.com/fda-revokes-roche-emergency-use-authorization-on-zika-test/
- Published: 2017-06-30T12:00:00.000Z
- Updated: 2026-09-14T22:32:40.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5139071

*Federal Register* notice: FDA has revoked an Emergency Use Authorization issued to Roche Molecular Systems for the LightMix Zika rRT–PCR Test. The revocation is based on a Roche request due to false positive test results. To view the notice, click [here](https://www.gpo.gov/fdsys/pkg/FR-2017-06-30/pdf/2017-13666.pdf?ref=fdaweb.com).