FDA found undeclared meloxicam in SILINTAN 25-pill bottles from Shanghai Chinese Medical Works. Recalled due to marketing without FDA approval. No specific remedy stated in official notice.
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
The FDA has recalled SILINTAN 25-pill bottles from Shanghai Chinese Medical Works because they contain undeclared meloxicam. This means the product was marketed without proper FDA approval, which could pose health risks.
The product was marketed without FDA approval and contains undeclared meloxicam, a medication that can cause serious health issues if misused. Meloxicam is not approved for use in this product, so it may interact with other medications or cause adverse effects.
People who purchased SILINTAN 25-pill bottles from Shanghai Chinese Medical Works in the U.S. are affected. Those with health conditions requiring meloxicam may be at higher risk.
Check for SILINTAN 25-pill bottles labeled 'Shanghai Chinese Medical Works' from 123Herbals LLC. All lots within expiry date are included in this recall.
Review the product label for the brand name 'Shanghai Chinese Medical Works' and product type 'SILINTAN 25/pills'.
The FDA found undeclared meloxicam in this product, which was marketed without approval. It may pose health risks, but the official notice does not specify a remedy.
The official recall notice does not state a remedy, so there is no specific instruction to stop using it.
Check the product label for 'SILINTAN 25/pills' from 'Shanghai Chinese Medical Works' and 123Herbals LLC.
We’ve drafted a message you can send 123Herbals LLC to request your refund or repair — edit it as you like.
Subject: Recall D-0388-2026 — 123Herbals LLC 123Herbals LLC Hello, I own a 123Herbals LLC that is covered by recall D-0388-2026 from 123Herbals LLC. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
