Drug recall
Source Plasma
FDA recall event 83079 · Class III · BioLife Plasma Services L.P.
Key facts
| Event ID | 83079 |
|---|---|
| Recall numbers | B-0714-2019 |
| Recalling firm | BioLife Plasma Services L.P. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma units, for which donor eligibility screening was incorrectly performed, were distributed. |
| Initiation date | May 15, 2019 |
| Report date | Aug 7, 2019 |
| Termination date | Jul 30, 2019 |
| City | Ankeny |
| State | IA |
| Country | United States |
| FEI number | 3011638482 |
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: