Drug recall
OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle…
FDA recall event 95511 · Class II · Akron Pharma, Inc.
Key facts
| Event ID | 95511 |
|---|---|
| Recall numbers | D-0025-2025 |
| Recalling firm | Akron Pharma, Inc. |
| Product type | Drugs |
| Products | 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… |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | CGMP Deviations |
| Initiation date | Oct 15, 2024 |
| Report date | Oct 30, 2024 |
| City | Fairfield |
| State | NJ |
| Country | United States |
| FEI number | 3013943804 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: