Drug recall
Cryoprecipitated AHF
FDA recall event 52256 · Class II · American National Red Cross (The)
Key facts
| Event ID | 52256 |
|---|---|
| Recall numbers | B-0627-13, B-0628-13, B-0629-13, B-0630-13, B-0631-13, B-0632-13 |
| Recalling firm | American National Red Cross (The) |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Plasma Frozen, Plasma Frozen 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, possibility sterility compromised and contaminated, were distributed. |
| Initiation date | Feb 12, 2009 |
| Report date | Jan 16, 2013 |
| Termination date | Jan 4, 2013 |
| City | Portland |
| State | OR |
| Country | United States |
| FEI number | 3072996 |
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: