Drug recall
Levothroid (levothyroxine sodium tablets, USP), 25 mcg, 100- and 1,000-tablet bottles, RX only, NDC…
FDA recall event 38274 · Class II · Lloyd Inc of Iowa
Key facts
| Event ID | 38274 |
|---|---|
| Recall numbers | D-962-2007, D-963-2007 |
| Recalling firm | Lloyd Inc of Iowa |
| Product type | Drugs |
| Products | Levothroid (levothyroxine sodium tablets, USP), 25 mcg, 100- and 1,000-tablet bottles, RX only, NDC 0456-1320-01 (100-ct.) and NDC 0456-1320-00 (1,000-ct.). Manufactured for Forest Pharmaceuticals…, Thyro-Tab 0.025mg, 150,000-tablet bulk drums intended for repackaging, Rx only. Manufacturer: Lloyd Pharmaceutical, Shenandoah, IA 51601. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent; 9 month stability, Subpotent; 9month stability |
| Initiation date | Jun 27, 2007 |
| Termination date | Aug 28, 2008 |
| City | Shenandoah |
| State | IA |
| Country | United States |
| FEI number | 1911196 |
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