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 American Health Packaging Due to Failed Dissolution Specifications: results were above specification.
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 American Health Packaging directly.
Affected Products
GlipiZIDE Extended-Release Tablets, 2.5 mg, 30 Tablets (3 blister cards each with 10 individually blistered doses), Rx only, Manufactured by: Patheon Pharmaceuticals Inc., Cincinnati, OH 45237; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054. Carton NDC#: 68084-295-21 (Individual Dose NDC: 68084-295-11)
Quantity: 2,266 cartons
Why Was This Recalled?
Failed Dissolution Specifications: results were above specification.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About American Health Packaging
American Health Packaging has 56 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report