Drug recall
25 mcg, NDC 60793-116-01, Cytomel, LIOTHYRONINE SODIUM TABLETS, 100 Tablets, Rx only*** Manufactured by King…
FDA recall event 52850 · Class II · King Pharmaceuticals Inc
Key facts
| Event ID | 52850 |
|---|---|
| Recall numbers | D-1895-2009 |
| Recalling firm | King Pharmaceuticals Inc |
| Product type | Drugs |
| Products | 25 mcg, NDC 60793-116-01, Cytomel, LIOTHYRONINE SODIUM TABLETS, 100 Tablets, Rx only*** Manufactured by King Pharmaceuticals, Inc., Bristol, TN 37630 |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Lot was found to be out of specification at the 12 month stability time point |
| Initiation date | Aug 6, 2009 |
| Termination date | May 20, 2010 |
| City | Bristol |
| State | TN |
| Country | United States |
| FEI number | 1000208638 |
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