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US COVID-19 Fraud: Home-Use Fingerstick Collection Kits Promised Results Within 72 Hours

 
• By Eileen Francis

FDA warns Florida firm Modern Allergy Management and a testing lab abut an unapproved and mislabeled home-use fingerstick sample collection for COVID-19 test. The firm promised results within three days.

blue blood lancet penetrates to the skin of left hand with white background (isolated and have clipping path)

The latest unapproved OTC sales the US Food and Drug Administration found of home-use sample collections for COVID-19 tests are for a fingerstick device marketed with a claim of providing results within three days.

The agency’s Center for Devices and Radiological Health sent a

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Tariffs on imports from China and look at eliminating self-affirmed GRAS pathway introduced under Trump while DoJ Consumer Protection Branch also continues supplement sector priorities enduring across administrations.

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Digital Services Deliver Hemp, States Deliver Regulation With Congress Yet To Act

 
• By Malcolm Spicer

Four months into session, no bills have been introduced in Congress to authorize FDA to establish a regulatory pathway for the lawful use of hemp ingredients in products other than drugs or propose some other solution to the federal conundrum present since lawmakers in 2018 de-scheduled hemp.

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• By Malcolm Spicer

Dyes and colors which FDA says industries agree should no longer be used aren’t unsafe and are currently used only with the agency’s approval, industry stakeholders say. Center for Science in the Public Interest says the dyes are used “in tens of thousands of foods and beverages that are commonly consumed here in the United States.”

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• By David Ridley

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