On 7 January 2026, Anthony Trinh, 123Herbals LLC, based in Rosemead, California, announced a voluntary consumer-level recall of all lots of Silintan capsules following findings by the U.S. Food and Drug Administration (FDA) that the product is tainted with meloxicam.
Meloxicam is an FDA-approved nonsteroidal anti-inflammatory drug (NSAID) indicated for the management of osteoarthritis pain. Products containing meloxicam cannot be legally marketed as dietary supplements. The presence of this active pharmaceutical ingredient renders Silintan capsules an unapproved new drug, for which safety and efficacy have not been established, making the product subject to recall under U.S. law.
Health Risk
According to the company, exposure to meloxicam at doses exceeding the recommended maximum of 15 mg/day may pose a reasonable probability of serious and potentially life-threatening adverse events, including blood clots, heart attack, and stroke. Additional risks include hypersensitivity reactions, gastrointestinal bleeding, ulceration, and perforation, as well as acute kidney injury, particularly among elderly individuals. Significant drugdrug interactions may also occur in consumers taking blood thinners or other NSAIDs, substantially increasing the risk of bleeding.
As of the recall announcement, no adverse events had been reported to 123Herbals LLC.
Product Details and Distribution
The recalled product, Silintan capsules, is marketed as a dietary supplement for relief of joint and body aches. It is packaged in 25-count plastic bottles with blue labels. The recall applies to all lot numbers within expiry. The product was distributed nationwide in the United States via online sales through 123herbals.com.
Consumer and Retailer Actions
Consumers and retailers are advised to stop using or selling the product immediately. Affected products should be returned to the place of purchase, discarded, or returned directly to the company. Consumers who have taken the product and have health concerns should seek medical advice promptly.
Company and FDA Actions
123Herbals LLC is notifying distributors and customers via email and arranging for returns of all recalled products. Consumers may contact the company at hello@123herbals.com
or by phone at +1-626-656-3202 (Monday to Friday, 8:00 a.m. to 5:00 p.m. Pacific Time). Customers who purchased the product online may return it to 300 West Valley Blvd., P.O. Box 1925, Alhambra, CA 91803 for a refund.
Consumers and healthcare professionals are encouraged to report adverse reactions or quality issues associated with this product to the FDAs MedWatch Adverse Event Reporting Program. The recall is being conducted with the knowledge of the U.S. Food and Drug Administration.