Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Valsartan 320 mg Tablets Recalled by RemedyRepack Inc. Due to CGMP Deviations: Carcinogen impurity detected in API used...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact RemedyRepack Inc. directly.
Affected Products
Valsartan 320 mg Tablets, HDPE 90 cc bottles in cardboard trays, Rx Only, RemedyRepack, Inc., 625 Kolter Drive, Suite 4, Indiana, PA 15701, NDC 61786-0793-19
Quantity: 36 bottles of 90 = 3240 tablets
Why Was This Recalled?
CGMP Deviations: Carcinogen impurity detected in API used to manufacture drug product.
Where Was This Sold?
This product was distributed to 2 states: FL, VA
About RemedyRepack Inc.
RemedyRepack Inc. has 60 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report