The US Food and Drug Administration issuedFDAWarning letters to 7 companies for illegally selling dietary supplements that claim to treat, mitigate, or prevent cardiovascular disease, or related conditions, such as atherosclerosis, stroke, or heart failure, in violation of the Federal Food, Drug and Cosmetic Act, and that According to the site “FDA“.
Warning to consumers
Urges the US Food and Drug Administration (FDA) Consumers not to use these or similar products because they have not been evaluated by the US FDA as safe or effective for their intended use and may be harmful. Warning letters have been issued to 7 companies.
site saidFDA“Because cardiovascular disease is the leading cause of death in the United States, it is important that the FDA protects the public from products and companies that make illegal claims to treat it.
Supplements warning
said Kara Welch, program director Nutritional supplements In the Authority’s Center for Food Safety and Applied Nutrition, “We encourage consumers to remain vigilant when shopping online or in stores to avoid purchasing products that may endanger their health.”.”
Under FDA law, products intended to diagnose, treat, mitigate or prevent disease are drugs and are subject to requirements that apply to drugs, even if they are classified as dietary supplements. Unlike drugs approved by the FDA, the agency has not evaluated whether products Unapproved subject to warning letters posted today are effective for their intended use, what the appropriate dose is, how they might interact with FDA-approved medications or other substances, or whether they have serious side effects or other safety concerns..
FDA warns 7 companies for selling unlicensed supplements
The US Food and Drug Administration advises(FDA) Consumers should talk to a doctor, pharmacist, or other healthcare provider before deciding to buy or use any dietary supplement or medication Some supplements may interact with other medications or supplements Healthcare providers will work with patients to determine the best treatment for their condition.
If a consumer believes a product has caused a reaction or illness, they should immediately stop using the product and contact their healthcare provider. The FDA encourages healthcare providers and consumers to report any adverse reactions associated with medicinal products or supplements.
supplements
FDA has requested responses from the companies within 15 business days explaining how they will address the issues described in the warning letters or provide their reasons and supporting information as to why they believe the products do not violate the law Failure to promptly correct violations may result in legal action, including forfeiture product, or other procedures.