Akron Pharma, Inc. recalls OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Phar
Recalled October 30, 2024 · FDA recall D-0025-2025 · Akron Pharma
Hazard
CGMP Deviations · FDA Class II
Units
10845 bottles
Sold at
Nationwide in the US
Description
CGMP Deviations
Product
OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., Fairfield, NJ 07004, NDC 71399-0039-06.
Manufacturer(s)
Akron Pharma, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →