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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted October 02, 2023
Dangerous Ingredients Found in Ten Arthritis and Pain Supplements
On September 29, 2023, the FDA warned consumers that the following arthritis and pain management products contain undeclared drugs such as diclofenac, methocarbamol (a muscle relaxant), and dexamethasone (a corticosteroid), and/or other potentially harmful ingredients. Use the links below for more information about each product.
- Kuka Flex Forte
- Reumo Flex
- Tapee Tea (see previous warning)
- Fast-Act Rheuma Capsule
- New Fast-Act Rheumatism Capsule
- UA-Block
- AK Forte
- Artri King (see previous warning)
- Ortiga Mas Ajo Rey (see previous warning)
- Ortiga Mas Ajo Rey Extra Forte (see previous warning)
Undeclared drugs and other ingredients in these products can cause adverse effects such as low blood pressure, sedation and dizziness, infections, increased blood sugar, bone damage, and psychiatric problems. Consumers who have been taking these products should consult with their healthcare provider before discontinuing, as suddenly stopping corticosteroids after long-term use can result in withdrawal syndrome.
Consumers and healthcare providers can report any adverse reactions to the FDA’s MedWatch Voluntary Reporting Program.
See ConsumerLab’s Review of Joint Health Supplements for more information about related products.
Also see ConsumerLab’s article about supplements promoted to help with arthritis.
For more information, use the link below.
Tainted Arthritis | Pain Products
See related recalls and warnings:
Walmart Inc. Recalls Joint Supplements With Omega-3, Glucosamine & CurcuminWalmart Inc. Recalls Joint Supplements With Omega-3, Glucosamine & Curcumin
Prescription Drugs Found in Arthritis, Muscle Pain, and Osteoporosis Supplements
Pharmaceutical Drugs Found In Dietary Supplements Pose Danger to Consumers
Recall: Arthritis and Muscle Pain Supplement Contains Prescription Drugs
Arthritis Supplement Containing Multiple Drugs Recalled
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.
