Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
PONSTEL (Mefanamic Acid) USP Recalled by Shionogi Inc. Due to Failed Dissolution Specifications: Low dissolution results were obtained...
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
PONSTEL (Mefanamic Acid) USP, 250 mg capsules, 30-count bottles, Rx Only, Manufactured for: Shionogi Inc. Florham Park, NJ 07932 Manufactured by: Halo Pharmaceutical Inc. Whippany, NJ 07981
Quantity: 455 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.
About Shionogi Inc.
Shionogi Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report