Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 66066 · Class II, Class III · Gulf Coast Regional Blood Center
Key facts
| Event ID | 66066 |
|---|---|
| Recall numbers | B-0659-15, B-0660-15, B-0661-15, B-0662-15, B-0663-15, B-0664-15, B-0665-15, B-0666-15, B-0667-15, B-0668-15, B-0669-15, B-0670-15 and 1 more |
| Recalling firm | Gulf Coast Regional Blood Center |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Cryoprecipitated AHF, Cryoprecipitated AHF, Pooled, Fresh Frozen Plasma (Apheresis), Plasma Frozen Cryoprecipitate Reduced and 8 more |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from ineligible donors, were distributed. |
| Initiation date | Jun 14, 2013 |
| Report date | Jul 1, 2015 |
| Termination date | May 11, 2017 |
| City | Houston |
| State | TX |
| Country | United States |
| FEI number | 3002133806 |
At a glance
- 10–99 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: