Drug recall
Senokot (standardized senna concentration) Tablets, 8.6 sennosides, 50 count bottles, The Purdue Frederick…
FDA recall event 29956 · Class III · The Purdue Frederick Company
Key facts
| Event ID | 29956 |
|---|---|
| Recall numbers | D-281-4 |
| Recalling firm | The Purdue Frederick Company |
| Product type | Drugs |
| Products | Senokot (standardized senna concentration) Tablets, 8.6 sennosides, 50 count bottles, The Purdue Frederick Company, Norwalk, CT 06850-3590, NDC 0034-1200-50 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Mispackaging: Two orange Senokot-S tablets found within a bottle of Senokot Tablets (brown tablets). |
| Initiation date | Sep 2, 2004 |
| 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