Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due to Presence of Foreign substance: identified as a dead...
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
Cefdinir for Oral Suspension USP, 125 mg/5mL, packaged in a) 60 mL bottle (NDC 68180-722-20), b) 100 mL bottle (NDC 68180-722-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mandideep 462 046 INDIA
Quantity: a) 4074 bottles b) 30,300 bottles
Why Was This Recalled?
Presence of Foreign substance: identified as a dead ant.
Where Was This Sold?
Product was distributed to major distributors/wholesalers throughout the United 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