Drug recall
Liquid Plasma
FDA recall event 89344 · Class II · American National Red Cross (the)
Key facts
| Event ID | 89344 |
|---|---|
| Recall numbers | B-0147-2022, B-0148-2022, B-0149-2022, B-0150-2022 |
| Recalling firm | American National Red Cross (the) |
| Product type | Biologics |
| Products | Liquid Plasma, PF24 Plasma, Plasma Frozen, Cryoprecipitate Reduced, Red Blood Cells, Leukocytes Reduced |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary: Firm Initiated |
| Reason for recall | Blood products, collected in a manner that may have compromised the sterility of the collection system, were distributed. |
| Initiation date | Jul 17, 2021 |
| Report date | Jan 26, 2022 |
| Termination date | Jan 18, 2022 |
| City | West Henrietta |
| State | NY |
| Country | United States |
| FEI number | 3002957282 |
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: