Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Ongoing Initiated Apr 26, 2023 (3 years ago)

Valproic Acid Oral Solution

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

Why it was recalled

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

Cause type: Stability / shelf life

The product degraded or failed stability testing before its labeled expiry. Heat, moisture or time can break the drug down into degradants or reduce potency. All stability / shelf life recalls.

What was recalled

Valproic Acid Oral Solution, USP, 250mg/5mL, 473 mL bottles, Rx only, Distributed by: Akorn Operating Company LLC, Gurnee, IL 60031. ALL NDCs

Drug: Valproic

Recalling firm
Akorn, Inc.
Origin
IL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0854-2023 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall.

Other Valproic recalls

See all
Class II · Moderate risk

Valproic Acid Oral Solution

CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.

Terminated Microbial contamination American Health Packaging D-0854-2021
Class II · Moderate risk

Valproic Acid Oral Solution USP

CGMP Deviations: Potential concern with products manufactured using liquid sugar batches contaminated with microbial organisms.

Completed Microbial contamination Morton Grove Pharmaceuticals, Inc. D-0816-2021
Class III · Low risk

Divalproex Sodium Delayed-Release Tablets

Labeling: Label Error On Declared Strength; Some bottles of product were missing the color-coded strength on the primary display panel of the label.

Terminated Labeling / mix-up Upsher Smith Laboratories, Inc. NDC 0245-0182-11 D-127-2013

Other recalls by Akorn, Inc.

All 2023 recalls