Diovan (valsartan) Medication Recall
HOPE Clinic
Aug 31
1 min read
Medication recall announcement
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
Product Quantity: N/A
Recall Number:
D-0746-2026
Code Information:
Lot AV5913C, Expiry: 6/2027
Classification:
Class II
Event Details
Event ID:
99552
Voluntary / Mandated:
Voluntary: Firm initiated
Product Type:
Drugs
Initial Firm Notification of Consignee or Public:
Letter
Status:
Ongoing
Distribution Pattern:
US Nationwide
Recalling Firm:
Novartis Pharmaceuticals Corporation 1 Health Plz
East Hanover, NJ 07936-1016
United States
Press Release URL(s):
Press Release Not Issued For This Recall
Recall Initiation Date:
8/4/2026
Center Classification Date:
8/7/2026
Date Terminated:
N/A
*N/A - Not Available