Drug recall
Senokot-S Tablets (Docusate sodium 50mg and Sennosides 8.6mg) Natural Vegetable Laxative plus Softener…
FDA recall event 25896 · Class III · The Purdue Frederick Company
Key facts
| Event ID | 25896 |
|---|---|
| Recall numbers | D-224-3 |
| Recalling firm | The Purdue Frederick Company |
| Product type | Drugs |
| Products | Senokot-S Tablets (Docusate sodium 50mg and Sennosides 8.6mg) Natural Vegetable Laxative plus Softener, Standardized Senna Concentrate and Docusate Sodium, blisterpack of 4 tablets, Professional… |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mislabeled; Labeling does not indicate dosage instructions for children under 2 years of age |
| Initiation date | Mar 11, 2003 |
| City | Stamford |
| Country | United States |
| FEI number | 1250012 |
At a glance
- 1–9 Products in this recall
- None 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