Drug recall
Blood and Blood Products for Reprocessing
FDA recall event 78723 · Class II, Class III · Blood Systems, Inc. dba Lifeblood
Key facts
| Event ID | 78723 |
|---|---|
| Recall numbers | B-0244-2018, B-0245-2018 |
| Recalling firm | Blood Systems, Inc. dba Lifeblood |
| Product type | Biologics |
| Products | Blood and Blood Products for Reprocessing, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II, Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Blood products, collected from a donor in which donor suitability was not adequately determined, were distributed. |
| Initiation date | Nov 9, 2017 |
| Report date | Jan 17, 2018 |
| Termination date | Jan 5, 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: