Drug recall
Cryoprecipitated AHF
FDA recall event 69212 · Class II · HCSC-Blood Center
Key facts
| Event ID | 69212 |
|---|---|
| Recall numbers | B-0964-14, B-0965-14, B-0966-14, B-0967-14, B-0968-14, B-0969-14 |
| Recalling firm | HCSC-Blood Center |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Fresh frozen plasma, Plasma cryoprecipitate reduced, Red Blood Cells, Red blood cells leukocytes reduced and 1 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected in a manner that may have compromised the sterility of the collection system, were distributed. |
| Initiation date | Feb 23, 2010 |
| Report date | Sep 24, 2014 |
| Termination date | Sep 12, 2014 |
| City | Bethlehem |
| State | PA |
| Country | United States |
| FEI number | 2573135 |
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: