Class III โ€” Low Risk

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

Mefenamic Acid Recalled by Shionogi Inc. Due to Failed Dissolution Specifications: Low dissolution results were obtained...

Date: May 24, 2017
Company: Shionogi 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 Shionogi Inc. directly.

Affected Products

Mefenamic Acid, 250mg capsules, packaged in 30-count bottles, Rx Only, Distributed by: Prasco Laboratories Mason, OH 45040 USA, Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981, NDC 66993-070-30

Quantity: 6304 bottles

Why Was This Recalled?

Failed Dissolution Specifications: Low dissolution results were obtained during stability testing

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Shionogi Inc.

Shionogi Inc. has 5 total recalls tracked by RecallDetector.

Related Recalls

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