Drug recall
Cornea
FDA recall event 71581 · Class I · OneLegacy
Key facts
| Event ID | 71581 |
|---|---|
| Recall numbers | B-0751-15 |
| Recalling firm | OneLegacy |
| Product type | Biologics |
| Products | Cornea |
| Classification | Class I |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human corneas, not tested adequately and appropriately to reduce the risk of transmission of relevant communicable diseases, were distributed. |
| Initiation date | Apr 25, 2015 |
| Report date | Aug 19, 2015 |
| Termination date | Aug 7, 2015 |
| 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: