Drug recall
Apheresis Platelets, Leukocytes Reduced
FDA recall event 80988 · Class II · Belle Bonfils Memorial Blood Center
Key facts
| Event ID | 80988 |
|---|---|
| Recall numbers | B-0805-2018 |
| Recalling firm | Belle Bonfils Memorial Blood Center |
| Product type | Biologics |
| Products | Apheresis Platelets, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Apheresis product, in which platelet yield did not meet specifications, was distributed. |
| Initiation date | Jul 29, 2018 |
| Report date | Sep 26, 2018 |
| Termination date | Sep 17, 2018 |
| City | Denver |
| State | CO |
| Country | United States |
| FEI number | 3000210247 |
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: