Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Suprax Recalled by Lupin Pharmaceuticals Inc. Due to Failed Impurities/Degradation Specifications: Product did not meet 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 Lupin Pharmaceuticals Inc. directly.
Affected Products
Suprax, Cefixime for Oral Suspension USP, 500 mg/5 ml, 20 mL (when reconstituted), Rx only, Manufactured for Lupin Pharmaceuticals, Inc. 111 South Calvert Street, Baltimore, MD 21202, Manufactured by Lupin Limited Mumbai 400 058 India, NDC 27437-207-03.
Quantity: 5,172 bottles
Why Was This Recalled?
Failed Impurities/Degradation Specifications: Product did not meet specification in total impurities at the 9-month stability station.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals Inc. has 119 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report