CLASS II Drug recall · Reported 5 Jun 2024 · FDA Enforcement Report

Cefdinir for Oral Suspension USP, 250 mg recalled

Lupin Pharmaceuticals is recalling Cefdinir for Oral Suspension USP, 250 mg, distributed nationwide in the US. The recall was initiated on 8 May 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #F305184, F305185, F305186, Exp 7/31/ 2025

NDC68180-722, 68180-723

UPC0368180723042

Quantity recalled51,006 bottles

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number: D-0518-2024
FDA event ID: 94602
Recalling firm: Lupin Pharmaceuticals, Baltimore, MD
Brand: Cefdinir
Manufacturer: Lupin Pharmaceuticals, Inc.
Classification: Class II
Status: Terminated
Recall initiated: 8 May 2024
FDA classified: 29 May 2024
Reported: 5 Jun 2024
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Packaging Defects
Drug class: Antibiotics

Timeline

8 May 2024	Recall initiated by company
29 May 2024	Classified by FDA	+21 days
5 Jun 2024	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Defective container: lack of seal integrity.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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

Where it was distributed

USA Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Defective container: lack of seal integrity.

Which lots are affected?

Lot #F305184, F305185, F305186, Exp 7/31/ 2025

Where was it sold?

USA Nationwide

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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Other Cefdinir recalls

All 11

Reported	Class	Recall	Company	Reason	Where
22 May 2024Drug	CLASS II	Cefdinir for Oral Suspension USP 125 mg/ when reconstituted) recalledCefdinir	Lupin Pharmaceuticals	Foreign Material	Nationwide
22 May 2024Drug	CLASS II	Cefdinir for Oral Suspension USP 250 mg/ when reconstituted) recalledCefdinir	Lupin Pharmaceuticals	Foreign Material	Nationwide
29 Jul 2020Drug	CLASS II	Cefdinir for Oral Suspension USP, 250 mg recalledCefdinir	Lupin Pharmaceuticals	Potency & Assay	Nationwide
13 Nov 2019Drug	CLASS III	Cefdinir for Oral Suspension USP, 125 mg recalledCefdinir	Lupin Pharmaceuticals	Packaging Defects	Nationwide
13 Nov 2019Drug	CLASS III	Cefdinir for Oral Suspension USP, 250 mg recalledCefdinir	Lupin Pharmaceuticals	Other	Nationwide