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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted December 22, 2021
Unauthorized Rapid Antigen Test Gets FDA Warning
On December 1, 2021, the FDA issued a warning letter for DermaCare Biosciences, LTD. following a review of the company's websites and social media, which found the company promoted the sale of the Easy Rapid Now COVID-19 Nasal Swab Antigen Test without marketing approval, clearance, or authorization from the FDA, making the product adulterated and misbranded.
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If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
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If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
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If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
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