Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fosinopril Sodium and Hydrochlorothiazide Tablets Recalled by Sandoz Inc Due to Subpotent; Hydrochlorothiazide at the 9 month time point.
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 Sandoz Inc directly.
Affected Products
Fosinopril Sodium and Hydrochlorothiazide Tablets, 10 mg/12.5 mg, Rx Only, 100 Tablets, Sandoz Inc. Princeton, NJ 08540 ---NDC 0185-0341-01,
Quantity: 2,491 bottles of 100 tablets each
Why Was This Recalled?
Subpotent; Hydrochlorothiazide at the 9 month time point.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Sandoz Inc
Sandoz Inc has 30 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report