Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc 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 Actavis Inc directly.
Affected Products
Glipizide 2.5 mg Extended-release tablets, 30-count bottle, Rx Only, Manufactured By: Patheon Pharmaceuticals Inc Cincinnati, OH 45237, NDC 00591-0900-30
Quantity: 167,152 bottles
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 Actavis Inc
Actavis Inc has 17 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report