Drug recall

Recovered Plasma

FDA recall event 37075 · Class II, Class III · Central Indiana Regional Blood Center, Inc

Key facts

Event ID 37075
Recall numbers B-0789-7, B-0790-7
Recalling firm Central Indiana Regional Blood Center, Inc
Product type Biologics
Products Recovered Plasma, 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 who was taking the drug Aricept, were distributed.
Initiation date Sep 8, 2006
Termination date Mar 22, 2007
City Indianapolis
Country United States
FEI number 1873403

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

Browse all FDA drug and product recalls