Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 61992 · Class II · Blood Assurance Inc
Key facts
| Event ID | 61992 |
|---|---|
| Recall numbers | B-2009-12, B-2010-12, B-2011-12, B-2012-12, B-2013-12, B-2014-12, B-2015-12 |
| Recalling firm | Blood Assurance Inc |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Cryoprecipitated AHF, Pooled, Fresh Frozen Plasma, Plasma Cryoprecipitated Reduced, Plasma Frozen within 24 hours (FP24) and 2 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor who was at risk for variant Creutzfeldt-Jakob disease (vCJD), were distributed. |
| Initiation date | May 1, 2012 |
| Report date | Jul 4, 2012 |
| Termination date | Jun 28, 2012 |
| City | Chattanooga |
| State | TN |
| Country | United States |
| FEI number | 1044860 |
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: