Drug recall
Senna Laxative (Standardized Senna Concentrate) sennosides 8.6 mg. per Tablets, OTC, packaged under…
FDA recall event 50080 · Class III · L. Perrigo Co.
Key facts
| Event ID | 50080 |
|---|---|
| Recall numbers | D-105-2009 |
| Recalling firm | L. Perrigo Co. |
| Product type | Drugs |
| Products | Senna Laxative (Standardized Senna Concentrate) sennosides 8.6 mg. per Tablets, OTC, packaged under distributor labels: Equaline brand, 250 tablets, NDC 41163-021-85, 100 tablets, NDC 41163-021-78 and… |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Superpotent; (senna concentrate) |
| Initiation date | Oct 21, 2008 |
| Termination date | Nov 16, 2009 |
| City | Allegan |
| State | MI |
| Country | United States |
| FEI number | 1811666 |
At a glance
- 1–9 Products in this recall
- 10–99 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