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.

univasc (moexipril HCl) tablets Recalled by Ucb, Inc Due to Failed Dissolution Testing: Failed 24 month dissolution testing.

Date: July 24, 2015
Company: Ucb, Inc
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 Ucb, Inc directly.

Affected Products

univasc (moexipril HCl) tablets, 7.5 mg, 100 Ct Bottle, Rx Only. Manufactured for UCB, Inc., Smyrna, GA 30080. NDC: 0091-3707-01.

Quantity: 2,916 Bottles

Why Was This Recalled?

Failed Dissolution Testing: Failed 24 month dissolution testing.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Ucb, Inc

Ucb, Inc has 2 total recalls tracked by RecallDetector.

Related Recalls

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