FDAFDA · Food and drugs·Recall number D-0746-2026
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
Published August 19, 2026 · Recall initiated: August 4, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Dissolution Specifications
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIOVAN
- Manufacturer
- Novartis Pharmaceuticals Corporation
- Distributor
- US Nationwide
- Lot
- Lot AV5913C, Expiry: 6/2027
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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