Drug recall
Plasma Frozen
FDA recall event 88236 · Class II · Versiti Indiana Inc
Key facts
| Event ID | 88236 |
|---|---|
| Recall numbers | B-0522-2021 |
| Recalling firm | Versiti Indiana Inc |
| Product type | Biologics |
| Products | Plasma Frozen |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Frozen Plasma, which tested repeat reactive (RR) for Hepatitis, was distributed. |
| Initiation date | Jun 24, 2021 |
| Report date | Jul 28, 2021 |
| Termination date | Jul 21, 2021 |
| City | Indianapolis |
| State | IN |
| Country | United States |
| FEI number | 1873403 |
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: