Drug recall
Levothyroxine sodium tablets, USP, 0.4 mg., RX, packaged under the following product names and package sizes…
FDA recall event 60257 · Class II · Lloyd Inc
Key facts
| Event ID | 60257 |
|---|---|
| Recall numbers | V-031-2012 |
| Recalling firm | Lloyd Inc |
| Product type | Veterinary |
| Products | Levothyroxine sodium tablets, USP, 0.4 mg., RX, packaged under the following product names and package sizes: (1) LLOYD Thyro-Tabs, packaged in 120-tablet btls, NDC 11789-254-10, LLOYD, Inc… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The recalled product may not maintain potency throughout its labeled shelf-life. |
| Initiation date | Oct 27, 2011 |
| Termination date | Mar 26, 2014 |
| 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