Drug recall
Cornea
FDA recall event 93660 · Class II · Eversight
Key facts
| Event ID | 93660 |
|---|---|
| Recall numbers | B-0102-2024 |
| Recalling firm | Eversight |
| Product type | Biologics |
| Products | Cornea |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Corneas, in which donor testing was conducted with an unacceptable sample, were distributed. |
| Initiation date | Jun 15, 2023 |
| Report date | Jan 3, 2024 |
| Termination date | Dec 28, 2023 |
| City | Ann Arbor |
| State | MI |
| Country | United States |
| FEI number | 3000718321 |
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 · Source date: