Class III โ€” Low Risk

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

Mercaptopurine Tablets Recalled by Stason Pharmaceuticals, Inc. Due to Failed Dissolution Specifications: results slightly under spec at...

Date: February 9, 2024
Company: Stason Pharmaceuticals, 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 Stason Pharmaceuticals, Inc. directly.

Affected Products

Mercaptopurine Tablets, USP 50 mg, packaged in: a) 25-count bottle (NDC 69076-913-02), b) 250-count bottle (NDC 69076-913-25), Rx only, Manufactured for: Quinn Pharmaceuticals, Boca Raton, FL, www.quinnrx.com

Quantity: 54, 131 bottles

Why Was This Recalled?

Failed Dissolution Specifications: results slightly under spec at at 9-months.

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Stason Pharmaceuticals, Inc.

Stason Pharmaceuticals, Inc. has 2 total recalls tracked by RecallDetector.

Related Recalls

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