Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GlipiZIDE Extended-release tablets Recalled by Amerisource Health Services Due to Failed dissolution specifications: Glipizide 2.5 mg ER Tablets...
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 Amerisource Health Services directly.
Affected Products
GlipiZIDE Extended-release tablets, 2.5 mg, 30-count carton (NDC 68084-295-21), Individual dose (NDC 68084-395-11), Rx Only, Packaged and Distributed by American Health Packaging, Columbus, Ohio 43217, NDC 68084-295-21
Quantity: 19,393 cartons (581,790 extended release tablets)
Why Was This Recalled?
Failed dissolution specifications: Glipizide 2.5 mg ER Tablets exceeded dissolution specification rates for the 10 hour testing point.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Amerisource Health Services
Amerisource Health Services has 23 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report