Good Lifestyle

It is not uncommon to include taking a supplement as part of your daily routine. Unlike prescription or over -the -counter drugs And health products, customers are looking for them to help stimulate their contribution from specific vitamins and minerals, make sure they sleep resting at night and will feed their fitness patterns. But now, Food & Drug Administration (FDA) has issued new warnings on several supplements which had just been recalled. Read more to see why products pose serious health problems.

Read this then: 2.5 million pounds of meat recalled on contamination fears, USDA warns .

On March 8, the FDA announced that the Natural Solutions Foundation had recalled that his Dr. Rima recommends the Nano Silver 10 ppm dietary supplement. The product was sold from January 22, 2020 to December 27, 2021.

The opinion indicates that the supplement makes unsurvited affirmations according to which it can be used to prevent, treat or cure Covid-19. He warns that "consumers who use this product instead of looking for a timely medical treatment run the risk of serious and potentially fatal consequences".

This decision comes just over a year after the Natural Solutions Foundation received an order from the Federal Court to Stop selling and distributing The deceptive product. The same organization previously was under fire For the sale of "nano silver" supplements during an Ebola epidemic which went to the United States in 2014, USA today reports. AE0FCC31AE342FD3A1346EBB1F342FCB

"The marketing of unproven products as treatments for COVID-19 endorses public health and violates the law" Brian M. Boynton , now the main deputy prosecutor of the civil division of the Ministry of Justice, said in a press release from the Ministry of Justice (DoJ) in 2021. "The ministry will work in close collaboration with the FDA to prevent anyone who Treck to take advantage of the pandemic by selling not approved, poorly extended drugs. "

As part of the DOJ order, the New Jersey -based organization must destroy any remaining stock of product and inform the recall customers. The FDA opinion specifies that customers have 22 days, on March 7, to fill out a response form and return any unused alternate for a refund. Customers with questions can also contact the Foundation by sending an e-mail address indicated in the recall notice.

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If you own a pet, you may want to take note of a second supplement reminder that has just been issued. On March 10, the FDA published an opinion announcing that Florida Stratford Care USA, Inc. Pulled his Omega-3 pet supplements sold under 61 different brand names.

The affected items were sold in lots of 60 flexible gel capsules wrapped in white plastic containers with "lot 31133 EXP 04/13/23" or "Lot 30837 Exp 10/26/22" printed at the bottom. The products were sold nationally through retailers and veterinary clinics and online by retailers, including Amazon and the animal -focused website, Chewy. A full list of product names can be found in the agency's opinion.

The company says that it has decided to recall pet products after discovering that they contain potentially high levels of vitamin A. As "general discomfort, anorexia, nausea, peeling skin, weakness, tremors, convulsions, paralysis and dead".

Customers who bought the assigned article are invited to stop feeding it immediately to their pets and to have it in a container where no other animals or fauna can eat it. Consumers can also contact the company for all questions and request a full refund for products.

This is not the only time when supplements or health products have been at the Center for FDA warnings. Last month, the agency announced that Volt candy had published a voluntary reminder for a batch of his male improvement capsules of Primezen Black 6000.

California based company said that it had issued the alert because the affected product contained Sildenafil and tadalafil not listed , who are inhibitors of phosphodiesterase (PDE-5) who are regulated by the FDA. The agency warned that the ingredients could interact with nitrates taken by people with diabetes, high blood pressure, high cholesterol or heart disease and lead to potentially fatal drop in blood pressure.

Even prescription drugs have been affected. On February 1, the FDA announced that IBSA Pharma Inc. had published a voluntary reminder for 27 lots of his medication in oral soil solution (levothyroxine sodium). The company said that it had drawn the affected product - which is generally prescribed to treat hypothyroidism as a replacement therapy - after discovering that the lots in question could be lower that listed on its packaging.

The company warned that the underpiratory product could lead patients to start to feel the immediate symptoms of hypothyroidism, in particular "fatigue, increased sensitivity to cold, constipation, dry skin, swollen face, loss of hair, slow heart rate, depression, swelling of the gland thyroid and / or gain of unexplained weight or difficulty losing weight. "The opinion advised all customers to take the medication to speak to their supplier health care to discuss a possible replacement.