Drug recall
Red Blood Cells Pheresis, Leukocytes Reduced
FDA recall event 33618 · Class III · Lifesource
Key facts
| Event ID | 33618 |
|---|---|
| Recall numbers | B-0182-6 |
| Recalling firm | Lifesource |
| Product type | Biologics |
| Products | Red Blood Cells Pheresis, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, which was labeled leukoreduced but was not tested to determine the white blood cell count as required in the firm's standard operating procedures, was distributed. |
| Initiation date | Aug 18, 2005 |
| Termination date | Nov 17, 2005 |
| City | Glenview |
| Country | United States |
| FEI number | 1472204 |
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