Akron Pharma, Inc.: OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL)
Recall reason: CGMP Deviations. Recalled by Akron Pharma, Inc.. Distribution: Nationwide in the US. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot #ODS230001A, ODS230002A, Exp. 10/2025; ODS230003A, Exp. 11/2025.. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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