Drug recall
Levothroid (levothyroxine sodium tablets, USP), 25 mcg., packaged in 100 and 1,000-tablet bottles, RX, NDC…
FDA recall event 36881 · Class II · Lloyd Inc of Iowa
Key facts
| Event ID | 36881 |
|---|---|
| Recall numbers | D-419-7, D-420-7 |
| Recalling firm | Lloyd Inc of Iowa |
| Product type | Drugs |
| Products | Levothroid (levothyroxine sodium tablets, USP), 25 mcg., packaged in 100 and 1,000-tablet bottles, RX, NDC 0456-1320-01 (100-tab.) and NDC 0456-1320-00 (1,000-tab.), Manufactured for Forest…, Thyro-Tab 0.025 mg., packaged in 150,000-tablet bulk drums intended for repackaging, RX, Manufacturer: Lloyd Pharmaceutical, Shenandoah, IA. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent (9-month stability) |
| Initiation date | Nov 29, 2006 |
| 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