Drug recall
Cryoprecipitated AHF
FDA recall event 36249 · Class III · Heartland Blood Centers
Key facts
| Event ID | 36249 |
|---|---|
| Recall numbers | B-0416-7 |
| Recalling firm | Heartland Blood Centers |
| Product type | Biologics |
| Products | Cryoprecipitated AHF |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, which were not manufactured according to specifications, were distributed. |
| Initiation date | May 26, 2006 |
| Termination date | Dec 4, 2006 |
| City | Aurora |
| Country | United States |
| FEI number | 1470274 |
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