(ConservativeInsider.org) – Though over-the-counter supplements can be beneficial to people, one dietary supplement known as Infla-650 has been recalled by the Food and Drug Administration in July 2024 after they discovered the supplements were laced with illicit drugs.
The supplements, which cost $55 and are available in stores nationwide as well as on Amazon, were promoted as a drug that would help “soothe the joints” and keep bones healthy. According to the marketing for the supplement, the active ingredients were a “blend of ancient Indian herbs.”
However, upon testing the supplement, it was discovered that Infla-650 actually contains three drugs that are not included on the label, including acetaminophen, which is the active ingredient in Tylenol; Diclofenac, a nonsteroidal anti-inflammatory drug (NSAID), and Phenylbutazone, which is an NSAID that has been banned in the United States for use in humans since the 1980’s after several deaths were linked to its usage. None of these three drugs are eligible to be marketed as dietary supplements within the U.S.
Though both acetaminophen and diclofenac can be used on their own to treat pain, fever, or inflammation, without knowledge of the drug or dosing levels, it is possible that consumers could unintentionally overdose on these medications. People with certain health conditions, such as gastrointestinal disorders, are discouraged from taking any type of NSAID medication as they can cause serious gastrointestinal damage.
The FDA released a statement announcing the recall and described the drugs as a “serious threat” to consumers. The company that manufactured and sold the drugs is known as GURU INC. and is based in Georgia. GURU INC. voluntarily agreed to a recall and sent a notice out to customers by email to request that consumers return their packages for a refund. The company stated that consumers who are experiencing adverse side effects they believe may be related to the supplement should immediately contact their healthcare provider. Customers can also report any issues associated with the use of this product to the FDA’s MedWatch Adverse Event Reporting program.
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