Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Lisinopril Tablets USP Recalled by Sandoz Inc Due to Labeling: Incorrect or Missing Package Insert
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
Lisinopril Tablets USP, 30 mg, 100-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0185-0630-01
Quantity: 3,048 bottles ( 304,800 tablets)
Why Was This Recalled?
Labeling: Incorrect or Missing Package Insert
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