Class III โ€” Low Risk

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

MECLIZINE HYDROCHLORIDE TABLETS Recalled by Golden State Medical Supply Inc. Due to Failed Impurities/Degradation Specifications: Out of specification for impurities.

Date: November 25, 2015
Company: Golden State Medical Supply 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 Golden State Medical Supply Inc. directly.

Affected Products

MECLIZINE HYDROCHLORIDE TABLETS, 25 mg, Packaged in a) 100 ct Bottles (NDC: 60429-205-01) and b) 1000 ct Bottles (NDC: 60429-205-10), Rx Only. Manufactured by: Par Pharmaceuticals Companies Inc., Spring Valley, NY 10977. Packaged by: GSMS Incorporated, Carmarillo, CA 93012.

Quantity: a) 737 Bottles; b) 3863 Bottles

Why Was This Recalled?

Failed Impurities/Degradation Specifications: Out of specification for impurities.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Golden State Medical Supply Inc.

Golden State Medical Supply Inc. has 50 total recalls tracked by RecallDetector.

Related Recalls

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