Drug recall
Source Plasma
FDA recall event 82770 · Class II · Talecris Plasma Resources
Key facts
| Event ID | 82770 |
|---|---|
| Recall numbers | B-0602-2019 |
| Recalling firm | Talecris Plasma Resources |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Source Plasma, identified as unsuitable due to a collection deviation or unexpected event, was distributed. |
| Initiation date | Apr 16, 2019 |
| Report date | Jun 19, 2019 |
| Termination date | Jun 11, 2019 |
| City | Oklahoma City |
| State | OK |
| Country | United States |
| FEI number | 3005480118 |
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: