RecallDepth
Class II Ongoing

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.

This recall is currently active, issued October 30, 2024. It was issued by Akron Pharma, Inc..

Company
Akron Pharma, Inc.
Recall Initiated
October 15, 2024
Posted
October 30, 2024
Recall Number
D-0025-2025
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
10845 bottles
Firm Location
Fairfield, NJ, United States
Official Source
View on FDA website ↗

Reason for Recall

CGMP Deviations

Distribution

Nationwide in the US

Lot / Code Info

Lot #ODS230001A, ODS230002A, Exp. 10/2025; ODS230003A, Exp. 11/2025.

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