Drug recall
Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01…
FDA recall event 61252 · Class II · Lloyd Inc
Key facts
| Event ID | 61252 |
|---|---|
| Recall numbers | D-1394-2012, D-1395-2012 |
| Recalling firm | Lloyd Inc |
| Product type | Drugs |
| Products | Levothroid (levothyroxine sodium tablets, USP), 75 mcg., 100-count bottles, Rx only, NDC 0456-1322-01, Manufactured for Forest Pharmaceuticals, Inc., Subsidiary of Forest Laboratories, Inc., St…, Thyro-Tab.075 mg., packaged in bulk drums for repackaging. The firm name on the label is Lloyd Pharmaceutical, Shenandoah, Iowa 51601. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval. |
| Initiation date | Feb 24, 2012 |
| Report date | Jul 4, 2012 |
| Termination date | Jul 30, 2013 |
| 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 · Source date: