Drug recall
Elanco brand Micotil 300 Tilmicosin injection, USP. 300 mg tilmicosin, USP as tilmicosin phosphate per ml in…
FDA recall event 31030 · Class I · Lilly, Eli & Co.
Key facts
| Event ID | 31030 |
|---|---|
| Recall numbers | V-043-5 |
| Recalling firm | Lilly, Eli & Co. |
| Product type | Veterinary |
| Products | Elanco brand Micotil 300 Tilmicosin injection, USP. 300 mg tilmicosin, USP as tilmicosin phosphate per ml in 250 ml bottles; product AH023038W. |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The client information sheet, which warns of death if product is injected into humans, was not included in the package, although the warning is on the package itself. |
| Initiation date | Jan 25, 2005 |
| City | Indianapolis |
| Country | United States |
| FEI number | 1819470 |
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