ANTHONY TRINH and 123Herbals LLC are recalling Silintan (25 count) because FDA testing found it contains undeclared meloxicam. Meloxicam is a non-steroidal anti-inflammatory drug (NSAID) that was not listed on the label and is being marketed without FDA approval. Consumers should contact their healthcare provider or pharmacist if they have used this product.
The undeclared meloxicam can cause serious side effects, including gastrointestinal bleeding, cardiovascular risks like heart attack or stroke, and kidney damage. These risks are significantly increased for consumers already taking other NSAIDs or prescription blood thinners.
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Shanghai Chinese Medical Works, Shanghai, China; Recall #: D-0388-2026

Front of package, Silintan dietary supplement pills

Back of package, Silintan dietary supplement pills
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: FDA iRES · FDA Press Release · Raw API Response
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