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.

ARIPIPRAZOLE TABLETS Recalled by Golden State Medical Supply Inc. Due to FAILED DISSOLUTION SPECIFICATIONS: Possibility of out-of-specification (OOS) dissolution...

Date: November 17, 2020
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

ARIPIPRAZOLE TABLETS, 15 mg, 30-count. bottles, Rx Only, GSMS Incorporated, Manufactured by: Apotex Inc. Toronto, Ontario, Canada, Packaged by GSMS, Incorporated, Camarillo, CA 93012 USA, NDC #60429-449-30

Quantity: 11,922 bottles

Why Was This Recalled?

FAILED DISSOLUTION SPECIFICATIONS: Possibility of out-of-specification (OOS) dissolution limits for the remaining shelf life of the Aripiprazole Tablets

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