Drug recall
Red Blood Cells, Leukocytes Reduced
FDA recall event 80259 · Class III · Blood Systems, Inc. dba Lifeblood
Key facts
| Event ID | 80259 |
|---|---|
| Recall numbers | B-0637-2018 |
| Recalling firm | Blood Systems, Inc. dba Lifeblood |
| Product type | Biologics |
| Products | Red Blood Cells, Leukocytes Reduced |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood product, labeled with a combination of incorrect or missing information was distributed. |
| Initiation date | May 4, 2018 |
| Report date | Jul 4, 2018 |
| Termination date | Jun 26, 2018 |
| City | Memphis |
| State | TN |
| Country | United States |
| FEI number | 1076019 |
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: