CLASS II ONGOING Drug recall · Reported 7 Jun 2023 · FDA Enforcement Report

Hydrocortisone and Acetic Acid Otic Solution recalled by Akorn

Akorn is recalling Hydrocortisone and Acetic Acid Otic Solution, USP, distributed nationwide in the US. The recall was initiated on 26 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll Lots
Quantity recalledN/A

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-0810-2023
FDA event ID
91788
Recalling firm
Akorn, Gurnee, IL
Classification
Class II
Status
Ongoing
Recall initiated
26 Apr 2023
FDA classified
1 Jun 2023
Reported
7 Jun 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

26 Apr 2023Recall initiated by company
1 Jun 2023Classified by FDA+36 days
7 Jun 2023Published in enforcement report+6 days

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

Reason for recall

CGMP Deviations: Firm went out of business and could no longer continue stability studies.

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

Hydrocortisone and Acetic Acid Otic Solution, USP, 10 mL bottles, Rx Only, Distributed by: Akorn, Inc., Gurnee, IL 60031. ALL NDCs

Where it was distributed

Nationwide in the USA and Puerto Rico

Nationwide Puerto Rico

Questions about this recall

Is Hydrocortisone and Acetic Acid Otic Solution, USP recalled?

Yes. Akorn recalled Hydrocortisone and Acetic Acid Otic Solution, USP on 26 Apr 2023. The recall is Class II and its status is Ongoing. Recall number D-0810-2023.

Why was it recalled?

CGMP Deviations: Firm went out of business and could no longer continue stability studies.

Which lots are affected?

All Lots

Where was it sold?

Nationwide in the USA and Puerto Rico

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.

More recalls from Akorn

All 192

Other Hydrocortisone and acetic acid otic recalls

All 6