Skip to content
Back to recalls
Drug FDA Class I Ongoing Mislabeling

SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

ANTHONY TRINH, 123Herbals LLC Published Mar 11, 2026

Risk level

Class I

Dangerous or defective — could cause serious health problems or death.

Severity score 85/100

What should you do?

  • Check whether you have this product, using the lot codes, UPCs, and dates listed below.
  • Do not eat, serve, or sell the affected product.
  • Return it to the place of purchase for a refund, or throw it away in a sealed bag so people and animals can’t get to it.
  • Contact ANTHONY TRINH, 123Herbals LLC or your place of purchase with questions, and see the source record below for full details.
Reason for recall

Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.

Hazards

Undeclared meloxicam · primary

Affected products (1)

SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China

N/A

Lot codes: within
Code info: All lots within expiry

Affected areas

Nationwide

Timeline

  1. Initiated
    Oct 20, 2025
  2. Published
    Mar 11, 2026
Recall number
D-0388-2026
Agency
U.S. Food and Drug Administration
Country
US

FDA records come from the openFDA drug enforcement-report dataset — the agency's full weekly enforcement list. Most entries are not issued as consumer press releases, so they won't appear on fda.gov/recalls or in a web search. The source record link above resolves this exact recall by its number.