Drug recall
Source Plasma
FDA recall event 81435 · Class III · BioLife Plasma Services LP
Key facts
| Event ID | 81435 |
|---|---|
| Recall numbers | B-0121-2019 |
| Recalling firm | BioLife Plasma Services LP |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma, collected from a donor for whom donor suitability was not adequately determined, were distributed. |
| Initiation date | Aug 28, 2018 |
| Report date | Nov 21, 2018 |
| Termination date | Nov 13, 2018 |
| City | Cedar Rapids |
| State | IA |
| Country | United States |
| FEI number | 3010187885 |
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: