Drug recall
Source Plasma
FDA recall event 31671 · Class II · BioLife Plasma Services LP
Key facts
| Event ID | 31671 |
|---|---|
| Recall numbers | B-1107-5 |
| Recalling firm | BioLife Plasma Services LP |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, that tested negative for viral markers, but were collected from an unsuitable donor due to the receipt of tattoos and body piercings within 12 months of donation, were distributed. |
| Initiation date | May 23, 2003 |
| City | Deerfield |
| Country | United States |
| FEI number | 3004414580 |
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