Drug recall
Cornea
FDA recall event 83801 · Class II · One Legacy
Key facts
| Event ID | 83801 |
|---|---|
| Recall numbers | B-0885-2019 |
| Recalling firm | One Legacy |
| Product type | Biologics |
| Products | Cornea |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Initiation date | Aug 10, 2019 |
| Report date | Sep 25, 2019 |
| Termination date | Sep 16, 2019 |
| City | Los Angeles |
| State | CA |
| Country | United States |
| FEI number | 3010307860 |
At a glance
- 1–9 Products in this recall
- 1–9 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: