Drug recall
Cornea
FDA recall event 65936 · Class II · Donor Network of Arizona
Key facts
| Event ID | 65936 |
|---|---|
| Recall numbers | B-2203-13 |
| Recalling firm | Donor Network of Arizona |
| Product type | Biologics |
| Products | Cornea |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Human Cornea, recovered from a donor who was not properly assess for hemodilution, was distributed. |
| Initiation date | Jul 18, 2013 |
| Report date | Sep 18, 2013 |
| Termination date | Sep 9, 2013 |
| City | Phoenix |
| State | AZ |
| Country | United States |
| FEI number | 3003374197 |
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: