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.

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed Dissolution Specification; 12-Month stability interval.

Date: December 13, 2013
Company: Dr. Reddy's Laboratories, 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 Dr. Reddy's Laboratories, Inc. directly.

Affected Products

Dr. Reddy's Metoprolol Succinate Extended-Release Tablets USP, 50 mg 100 tablets Rx Only Mfd. By: Dr. Reddy's Laboratories Limited Bachepalli -500 090 INDIA NDC 55111-467-01

Quantity: 8,592 bottles

Why Was This Recalled?

Failed Dissolution Specification; 12-Month stability interval.

Where Was This Sold?

This product was distributed to 5 states: LA, MI, MS, MO, OH

Affected (5 states)Not affected

About Dr. Reddy's Laboratories, Inc.

Dr. Reddy's Laboratories, Inc. has 163 total recalls tracked by RecallDetector.

Related Recalls

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