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# Emergency Use Revoked for Luminex Zika Assay
- URL: https://www.fdaweb.com/emergency-use-revoked-for-luminex-zika-assay/
- Published: 2019-09-18T12:00:00.000Z
- Updated: 2026-09-15T01:50:44.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5145032

*Federal Register* notice: FDA has announced it has revoked an emergency use authorization issued to Luminex for the xMAP MultiFLEX Zika RNA Assay. The *in vitro* diagnostic device for detecting the zika virus was revoked aat the company's request because the product will no longer be marketed. To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2019-20327.pdf?ref=fdaweb.com).