FDA recall record

Cefdinir for Oral Suspension USP, 250 mg/5 mL recall — FDA D-0518-2024

Defective container: lack of seal integrity.

Class IIclassification
D-0518-2024official record ID
Jun 5, 2024report date

Recall record at a glance

Official recordD-0518-2024
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmLupin Pharmaceuticals Inc.
Report dateJun 5, 2024
Recall initiation dateMay 8, 2024
Quantity51,006 bottles
LocationBaltimore, MD, United States

Official product description

Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, MD 21202, Manufactured by: Lupin Limited, Mandideep, 462 046 India, NDC 68180-723-04

Why the product was recalled

Defective container: lack of seal integrity.

Distribution information

USA Nationwide

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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