Drug recall
Cryoprecipitated AHF
FDA recall event 42130 · Class II · Northern California Community Blood Bank
Key facts
| Event ID | 42130 |
|---|---|
| Recall numbers | B-1776-12, B-1777-12, B-1778-12, B-1779-12, B-1780-12, B-1781-12, B-1782-12, B-1783-12, B-1784-12 |
| Recalling firm | Northern California Community Blood Bank |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Fresh Frozen Plasma, Plasma, Platelets, Platelets Pheresis Leukocytes Reduced and 4 more |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from donors whose confirmatory syphilis testing was invalid, were distributed. |
| Initiation date | Apr 17, 2006 |
| Report date | Jul 25, 2012 |
| Termination date | Jul 13, 2012 |
| City | Eureka |
| State | CA |
| Country | United States |
| FEI number | 2970101 |
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: