FDA Warns to Watch for Fake COVID-19 Tests
MONDAY, March 23, 2020 (HealthDay Information) — Pretend in-house test kits for coronavirus are becoming promoted in the United States and could pose critical wellness risks, the U.S. Foodstuff and Drug Administration says.
“We want to inform the American community that, at this time, the Food and drug administration has not licensed any test that is offered to buy for tests by yourself at house for COVID-19,” claimed Food and drug administration Commissioner Dr. Stephen Hahn and Associate Commissioner for Regulatory Affairs Judith McMeekin.
They claimed the Food and drug administration sees the community wellness price in growing availability of harmless, accurate exams for COVID-19 that could consist of house collection and is actively doing work with test developers.
“Fraudulent wellness statements, exams and goods can pose critical wellness risks,” Hahn and McMeekin warned in an agency information launch. “They could maintain some clients from looking for treatment or delay needed professional medical remedy.”
If you feel you have signs and symptoms of COVID-19, the Food and drug administration claimed you ought to adhere to U.S. Centers for Illness Control and Avoidance tips and speak to your wellness treatment supplier. He or she will advise you about whether or not you ought to get analyzed and how to get an correct test.
“The Food and drug administration will consider correct motion to shield consumers from terrible actors who consider edge of a disaster to deceive the community by advertising and marketing exams that pose risks to affected person wellness,” Hahn and McMeekin claimed. “This could consist of issuing warning letters, seizures or injunctions.”
The agency has issued warning letters to corporations selling and selling faux test kits. It has also stepped up enforcement at ports of entry, such as international mail amenities, to reduce faux kits from other international locations from getting into the United States.
Customers who know about faux test kits for COVID-19 ought to report them to the Food and drug administration, the agency claimed.
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