Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Glimepiride Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP Deviations
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 Northwind Pharmaceuticals LLC directly.
Affected Products
Glimepiride Tablets, USP 4mg, packaged in a) 30-count bottles (NDC 51655-120-52), and b) 90-count bottles (NDC 51655-120-26), Rx Only, Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46203.
Quantity: a) 198 bottles; b) 22 bottles
Why Was This Recalled?
CGMP Deviations
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Northwind Pharmaceuticals LLC
Northwind Pharmaceuticals LLC has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report