Home / Recalls / Novartis Pharmaceuticals Corporation / D-0746-2026

D-0746-2026 Class II Ongoing

Recalled by Novartis Pharmaceuticals Corporation — East Hanover, NJ

FDA drug recall D-0746-2026 was initiated by Novartis Pharmaceuticals Corporation on August 4, 2026 and is designated Class II. Reason for recall: Failed Dissolution Specifications The recall status is ongoing.

Recall Details

Product Type: Drugs
Report Date: August 19, 2026
Initiation Date: August 4, 2026
Termination Date: N/A
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity

Product Description

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

Reason for Recall

Failed Dissolution Specifications

Distribution Pattern

US Nationwide

Code Information

Lot AV5913C, Expiry: 6/2027

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