Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Lisinopril Tablets Recalled by Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals Due to Failed Dissolution Specifications

Date: July 29, 2015
Company: Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals
Status: Terminated
Source: FDA (Drug)

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 Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals directly.

Affected Products

Lisinopril Tablets, USP, 40 mg, a) 45-count bottle (NDC 0603-4214-60), b) 500-count bottle (NDC 0603-4214-28), Rx Only, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811

Quantity: 8,705 bottles

Why Was This Recalled?

Failed Dissolution Specifications

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals

Vintage Pharmaceuticals LLC dba Qualitest Pharmaceuticals has 2 total recalls tracked by RecallDetector.

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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report