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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Latest Posted June 26, 2024
FDA Warns Consumers Not to Use Infla-650 Due to Undeclared Drugs
Acetaminophen is an over-the-counter (OTC) pain reliever that can cause a rare, but potentially fatal skin reaction, and, in large doses, liver damage. Diclofenac is a prescription non-steroidal anti-inflammatory drug (NSAID) that can cause serious cardiovascular events such as heart attack or stroke, as well as bleeding, ulceration, and fatal tears of the stomach and intestines, or liver toxicity.
Phenylbutazone is a non-steroidal anti-inflammatory drug (NSAID) that was discontinued for human use in the United States due to the risk of serious and life-threatening injuries, including bone marrow toxicity. People with anemia, a low white or red blood cell count, or decreased blood platelets may be at a greater risk of death or serious injury.
Infla-650 capsules (see product photos) are promoted as an herbal dietary supplement for pain and sold on various websites, including nutraherbusa.com, and potentially in some retail stores. The product’s herbal ingredients listed include ashwagandha, fenugreek seed, shilajit, and more.
Consumers and healthcare providers can report any adverse reactions to the FDA’s MedWatch Voluntary Reporting Program.
For more information, use the link below.
Infla-650 contains hidden drug ingredients
See related recalls and warnings:
FDA Warns Consumers Not to Use Tapee Tea
Toxic Herb Found In Weight Supplements
FDA Warns Consumers of Supplement Containing Prescription Anti-Inflammatory Drug
FDA Warns Consumers Not to Use Ossos-Sans Supplement for Joints
Drug Found in Umary Supplement
Report a Problem
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:
Dietary Supplement or Nutritional Product Problem Report
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.
Please complete the form below as accurately as possible. You may need to check the label on the product.
Thank you for submitting your report.
Generic Drug Problem Report
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.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
Thank you for submitting your report.
Other Recent Recalls & Warnings
For information about reporting serious reactions and problems with medical products to the U.S. Food and Drug Administration through its MedWatch reporting program, please visit the FDA MedWatch website.
