Drug recall

Recovered Plasma

FDA recall event 25663 · Class II · American Red Cross Blood Services

Key facts

Event ID 25663
Recall numbers B-0766-3, B-0767-3
Recalling firm American Red Cross Blood Services
Product type Biologics
Products Recovered Plasma, Red Blood Cells, Leukocytes Reduced
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood products, that tested negative for hepatitis, but were collected from an ineligible donor due to a history of hepatitis, were distributed.
Initiation date Jun 14, 2002
City West Henrietta
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.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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