Drug recall
SENNA-LAX TABLETS, 8.6 MG., (8.6 mg Sennosides) bulk drum, 40,000 tablets (est), Caution: For Manufacturing…
FDA recall event 27228 · Class III · PDK Labs, Inc
Key facts
| Event ID | 27228 |
|---|---|
| Recall numbers | D-028-4 |
| Recalling firm | PDK Labs, Inc |
| Product type | Drugs |
| Products | SENNA-LAX TABLETS, 8.6 MG., (8.6 mg Sennosides) bulk drum, 40,000 tablets (est), Caution: For Manufacturing, Processing, or Repackaging , PDK Labs, Inc., 45 Ricefield Lane Hauppauge, NY 11788 |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotency |
| Initiation date | Jul 23, 2003 |
| City | Hauppauge |
| Country | United States |
| FEI number | 2432932 |
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