Drug recall

Recovered Plasma

FDA recall event 36351 · Class II · The Blood Center

Key facts

Event ID 36351
Recall numbers B-0474-7, B-0475-7
Recalling firm The Blood Center
Product type Biologics
Products Recovered Plasma, Red Blood Cells
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who was at increased risk for new variant Creutzfeldt-Jakob Disease (nvCJD), were distributed.
Initiation date Jul 25, 2005
Termination date Jan 12, 2007
City New Orleans
Country United States
FEI number 2374536

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

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