Drug recall
Levothroid Tablets (levothyroxine sodium tablets, USP) 50 mcg., 100-ct. bottles, Rx Only, Forest…
FDA recall event 28130 · Class II · Forest Pharmaceuticals Inc
Key facts
| Event ID | 28130 |
|---|---|
| Recall numbers | D-129-4 |
| Recalling firm | Forest Pharmaceuticals Inc |
| Product type | Drugs |
| Products | Levothroid Tablets (levothyroxine sodium tablets, USP) 50 mcg., 100-ct. bottles, Rx Only, Forest Pharmaceuticals, Inc., subsidiary of Forest Laboratories, Inc, St. Louis, MO --- NDC 0456-0321-01 |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Subpotent |
| Initiation date | Jan 26, 2004 |
| City | Earth City |
| Country | United States |
| FEI number | 1921065 |
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