Drug recall
Source Plasma
FDA recall event 82472 · Class II · Octapharma Plasma Inc
Key facts
| Event ID | 82472 |
|---|---|
| Recall numbers | B-0500-2019 |
| Recalling firm | Octapharma Plasma Inc |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, collected in a manner that may compromise potency, was distributed. |
| Initiation date | Mar 8, 2019 |
| Report date | May 29, 2019 |
| Termination date | May 23, 2019 |
| City | Reynoldsburg |
| State | OH |
| Country | United States |
| FEI number | 3013156936 |
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: