CLASS II Drug recall · Reported 12 Jan 2022 · FDA Enforcement Report

Cefixime Capsules, 400 mg recalled by Ascend Laboratories

Ascend Laboratories is recalling Cefixime Capsules, 400 mg, distributed nationwide in the US. The recall was initiated on 21 Dec 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 20140293, Exp Dec 2021; 20141525, 20141526, 20141527, Exp Mar 2022; 20143019, 20143020, 20143021, 20143022, Exp July 2022; 20144759, 20144760, 20144761, Exp Nov 22
NDC67877-584
Quantity recalled42,698 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-0359-2022
FDA event ID
89259
Recalling firm
Ascend Laboratories, Parsippany, NJ
Manufacturer
Ascend Laboratories, LLC
Classification
Class II
Status
Terminated
Recall initiated
21 Dec 2021
FDA classified
5 Jan 2022
Reported
12 Jan 2022
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

21 Dec 2021Recall initiated by company
5 Jan 2022Classified by FDA+15 days
12 Jan 2022Published 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

Failed impurities/degradation specifications

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Cefixime Capsules, 400 mg, 50-count bottles, Rx only, Manufactured by: Alkem Laboratories Ltd., Mumbai, India, Distributed by: Ascend Laboratories, LLC, Parsippany, NJ, NDC 67877-584-50

Where it was distributed

USA nationwide.

Nationwide

Questions about this recall

Is Cefixime Capsules, 400 mg recalled?

Yes. Ascend Laboratories recalled Cefixime Capsules, 400 mg on 21 Dec 2021. The recall is Class II and its status is Terminated. Recall number D-0359-2022.

Why was it recalled?

Failed impurities/degradation specifications

Which lots are affected?

Lot #: 20140293, Exp Dec 2021; 20141525, 20141526, 20141527, Exp Mar 2022; 20143019, 20143020, 20143021, 20143022, Exp July 2022; 20144759, 20144760, 20144761, Exp Nov 22

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 21 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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