Class III โ€” Low Risk

Low risk โ€” use of or exposure to this product is not likely to cause adverse health consequences.

Wockhardt Metoprolol Succinate Recalled by Wockhardt Usa Inc. Due to Failed Dissolution Specifications: Product was out of specification...

Date: April 17, 2014
Company: Wockhardt Usa 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 Wockhardt Usa Inc. directly.

Affected Products

Wockhardt Metoprolol Succinate, Extended-Release Tablets USP, 50 mg, a)100-count HDPE bottle (NDC 64679-735-02), b) 4000-count pack (64679-735-08), Manufactured by: Wockhardt Limited, Mumbai, India Distributed by Wockhardt USA LLC. 20 Waterview Blvd. Parsippany, NJ 07054 USA .

Quantity: 1,118,400 extended release tablets

Why Was This Recalled?

Failed Dissolution Specifications: Product was out of specification (OOS) at the 12 month long term stability testing point.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Wockhardt Usa Inc.

Wockhardt Usa Inc. has 45 total recalls tracked by RecallDetector.

Related Recalls

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