Reported Oct 30, 2024 · Ongoing
OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron…
Akron Pharma, Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Akron Pharma, Inc. · 373 Us Highway 46 Ste 117 · Fairfield, NJ · 07004-2456
Is this the product you have?
- OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Pharma
- Manufactured forAkron Pharma, Inc., Fairfield, NJ 07004, NDC 71399-0039-06
- Lot codes and dates
Lot #ODS230001AODS230002AExp. 10/2025ODS230003AExp. 11/2025
- Amount recalled
- 10845 bottles
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations
This product could cause temporary or reversible health problems — stop using it.
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