Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GLYBURIDE and METFORMIN HYDROCHLORIDE Tablets USP Recalled by Teva Pharmaceuticals USA Due to CGMP Deviations; laboratory testing was not followed in...
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
GLYBURIDE and METFORMIN HYDROCHLORIDE Tablets USP, 5mg/500mg, 500 count bottle, Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD harmaceuticals Ltd., Hinjwadi, Pune, India, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960, NDC: 0093-5712-05
Quantity: 2532 bottles
Why Was This Recalled?
CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements
Where Was This Sold?
This product was distributed nationwide across all 50 states.
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