US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 27, 2018 (8 years ago)

Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC…

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

Why it was recalled

Superpotent Drug

What was recalled

Lupin Cefdinir powder for Oral Suspension USP, 250 mg/5 mL in (a) 60 mL packs ( NDC 68180-723-20) and (b) 100 mL packs ( 68180-723-10), Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, Maryland 21202

Recalling firm
Lupin Pharmaceuticals Inc.
NDC code
68180-723-20
Origin
MD, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0684-2018

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.

Other Cefdinir recalls

See all