Akron Pharma recalls OneLAX Docusate Sodium Liquid due to CGMP deviations. Affected lots expire 10/2025 or 11/2025. No specific remedy stated in official notice.
CGMP Deviations
Akron Pharma is recalling OneLAX Docusate Sodium Liquid stool softener bottles due to manufacturing quality control issues. This recall does not pose a direct health risk but requires consumers to check their product details and contact the company for further instructions.
The product was manufactured with CGMP (Current Good Manufacturing Practice) deviations, which means the production process did not meet the required quality standards. This could potentially affect the product's safety and effectiveness, though the official notice does not specify a direct health hazard.
Anyone who owns or uses the OneLAX Docusate Sodium Liquid (50 mg/5 mL) stool softener bottle with lot numbers ODS230001A, ODS230002A, or ODS230003A. People taking this laxative for bowel regularity are most at risk if they have the affected lots.
Check the product label for the lot numbers ODS230001A, ODS230002A, or ODS230003A. The expiration dates for these lots are October 2025 or November 2025. The product is a 16 fl oz (473 mL) bottle of docusate sodium stool softener.
Look for lot numbers ODS230001A, ODS230002A, or ODS230003A on the bottle.
The official recall notice states there were CGMP deviations, but does not specify a direct health risk. Consumers should check their product details and contact Akron Pharma for further instructions.
The recall notice does not provide a specific remedy. You should check the product label for lot numbers and contact Akron Pharma for further instructions.
The affected lots expire in October 2025 or November 2025.
We’ve drafted a message you can send Akron to request your refund or repair — edit it as you like.
Subject: Recall D-0025-2025 — Akron Akron Hello, I own a Akron that is covered by recall D-0025-2025 from Akron. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
