Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
DOCU LIQUID (docusate sodium Recalled by Akorn, Inc. Due to CGMP Deviations: Firm went out of business and...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Akorn, Inc. directly.
Affected Products
DOCU LIQUID (docusate sodium, 50 mg/5 mL), packaged in 473mL bottles and b)10mL Unit Dose cups, Distributed by: Akorn Operating Company, LLC., Gurnee, IL 60031. ALL NDCs
Quantity: N/A
Why Was This Recalled?
CGMP Deviations: Firm went out of business and could no longer continue stability studies.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Akorn, Inc.
Akorn, Inc. has 176 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report