Drug recall
Source Plasma
FDA recall event 68694 · Class III · Grifols PlasmaCare, Inc.
Key facts
| Event ID | 68694 |
|---|---|
| Recall numbers | B-0859-14 |
| Recalling firm | Grifols PlasmaCare, Inc. |
| Product type | Biologics |
| Products | Source Plasma |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who disclosed history that warranted deferral or follow up and was not deferred or follow up questions were not asked, were distributed. |
| Initiation date | Jun 5, 2014 |
| Report date | Aug 13, 2014 |
| Termination date | Aug 5, 2014 |
| City | Milwaukee |
| State | WI |
| Country | United States |
| FEI number | 2176255 |
At a glance
- 1–9 Products in this recall
- 10–99 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: