Class I · Most seriousActive recall
SILINTAN 25/pills
A reasonable chance it could cause serious harm or death.
Does this affect you?
Check your lot numberAll lots within expiry
Where it was soldUSA nationwide
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.
What happened
Marketed Without an Approved NDA/ANDA: FDA analysis revealed the presence of undeclared meloxicam.
What to do
- Check the lot number and expiry on your medicine against the recall above.
- Talk to your pharmacist or doctor before changing anything — don't stop on your own.
- Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).
Who makes it
| Distributed by / for | ANTHONY TRINH, 123Herbals LLC |
Show the full FDA record
| Full product label | SILINTAN 25/pills, packaged in a 25-count bottle, Shanghai Chinese Medical Works, Shanghai, China |
| Recalling firm | ANTHONY TRINH, 123Herbals LLC |
| Distribution | USA nationwide |
| Quantity | N/A |
| Recall initiated | 2025-10-20 |
| Report date | 2026-03-11 |
| Recall completed | — |
| Recall number | D-0388-2026 |
| Classification | Class I |
| FDA status | Ongoing |
| Origin on file | Rosemead CA United States |
Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗
This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.