Class II · ModerateActive recall
Diovan
Could cause temporary or reversible harm; serious harm is unlikely.
Does this affect you?
Check your lot numberLot AV5913C, Expiry: 6/2027
Where it was soldUS 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
Failed Dissolution Specifications
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
Made byPatheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936
| Brand name | DIOVAN |
| Generic name | VALSARTAN |
| Active ingredient(s) | VALSARTAN |
| Distributed by / for | Novartis Pharmaceutical Corp, East Hanover, NJ 07936 |
| NDC | 0078-0359-34 |
Show the full FDA record
| Full product label | Diovan (valsartan) 160 mg, 90 tablets, Rx only, Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834, Distributed by: Novartis Pharmaceutical Corp, East Hanover, NJ 07936, NDC 0078-0359-34 |
| Recalling firm | Novartis Pharmaceuticals Corporation |
| Distribution | US Nationwide |
| Recall initiated | 2026-08-04 |
| Report date | 2026-08-19 |
| Recall completed | — |
| Recall number | D-0746-2026 |
| Classification | Class II |
| FDA status | Ongoing |
| Origin on file | East Hanover NJ 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.