Drug recall
Cryoprecipitated AHF
FDA recall event 58500 · Class II · Department of the Navy
Key facts
| Event ID | 58500 |
|---|---|
| Recall numbers | B-0076-15, B-0077-15, B-0078-15 |
| Recalling firm | Department of the Navy |
| Product type | Biologics |
| Products | Cryoprecipitated AHF, Fresh Frozen Plasma, Red Blood Cells |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, for which CMV testing was performed incorrectly, were distributed. |
| Initiation date | Feb 22, 2011 |
| Report date | Nov 26, 2014 |
| Termination date | Aug 25, 2016 |
| City | Washington |
| State | DC |
| Country | United States |
| FEI number | 1176560 |
At a glance
- 1–9 Products in this recall
- None 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: