Drug recall
Levothroid (levothyroxine sodium tablets, USP), 50 mcg, 100- and 1,000-tablet bottles, RX, NDC 0456-1321-01…
FDA recall event 37574 · Class II · Lloyd Inc of Iowa
Key facts
| Event ID | 37574 |
|---|---|
| Recall numbers | D-810-2007, D-811-2007 |
| Recalling firm | Lloyd Inc of Iowa |
| Product type | Drugs |
| Products | Levothroid (levothyroxine sodium tablets, USP), 50 mcg, 100- and 1,000-tablet bottles, RX, NDC 0456-1321-01 (100 tablets) and 0456-1321-00 (1,000 tablets). Manufactured for Forest Pharmaceuticals…, Thyro-Tab (levothyroxine sodium tablets), 0.050mg, 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 | Product may not maintain potency throughout labeled shelf life. |
| Initiation date | Feb 26, 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