Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Glipizide Extended-Release Tablets (anti-diabetic agent) Recalled by Teva Pharmaceuticals USA Due to Failed Moisture Limits: out of specification test results...
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 Teva Pharmaceuticals USA directly.
Affected Products
Glipizide Extended-Release Tablets (anti-diabetic agent), 5 mg, packaged in 30-unit dose blister pack per carton, Rx only, Mfd for: Watson Laboratories, Inc., Corona, CA 92880, Mfd by: Patheon Pharmaceuticals, Inc., Cincinnati, OH 43215, NDC 0591-0844-15
Quantity: 2,880 cartons (30 unit dose blister pack per carton)
Why Was This Recalled?
Failed Moisture Limits: out of specification test results for water content obtained during stability testing.
Where Was This Sold?
This product was distributed to 6 states: CT, IL, MI, OH, PA, VA
About Teva Pharmaceuticals USA
Teva Pharmaceuticals USA has 196 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report