Drug recall

Recovered Plasma

FDA recall event 30830 · Class II · American Red Cross Blood Services

Key facts

Event ID 30830
Recall numbers B-0695-5, B-0696-5
Recalling firm American Red Cross Blood Services
Product type Biologics
Products Recovered Plasma, Red Blood Cells, Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which tested negative for hepatitis, but were collected from an ineligible donor due to a reported history of hepatitis, were distributed.
Initiation date Apr 22, 2004
Termination date Mar 8, 2005
City Saint Louis
Country United States
FEI number 1973035

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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