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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted March 14, 2014
Arthritis and Muscle Pain Supplement Recalled
Recalled Reumofan Plus is promoted for the treatment of arthritis, muscle pain, osteoporosis, bone cancer and other conditions. It is packaged in a green and gold box of 30 tablets and was sold on nationwide through internet sales.
This product poses a serious health risk. Diclofenac is a non-steroidal anti-inflammatory (NSAID) drug that can increase the risk of cardiovascular events and gastrointestinal bleeding, and methocarbamol is a prescription muscle relaxant that can cause dizziness, low blood pressure and sedation.
Adverse events should be reported to the FDA's MedWatch Safety Information and Adverse Event Reporting Program.
The FDA first alerted consumers about the dangers of Reumofan Plus in June of 2012, and again in August 2012, after numerous adverse events were reported by consumers and tests revealed it contain prescription drugs.
Pain Free By Nature has ceased distribution of this product at this time.
See Related Warnings:
Recall: Arthritis and Muscle Pain Supplement Contains Prescription Drugs
FDA Warning on Supplement for Pain Relief
Dangerous Supplement Being Sold Under New Name
For more information about this recall, use the link below.
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.
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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.
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