US Drug Recall Register
Class II · Moderate risk Terminated Initiated Apr 24, 2024 (2 years ago)

Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.

What was recalled

Cefdinir for Oral Suspension USP 125 mg/5 mL (60 mL when reconstituted), 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202, United States, Manufactured by: Lupin Limited, Mandideep 462 046, India, NDC 68180-722-04

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
68180-722-04
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0497-2024

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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