Drug recall

Recovered Plasma

FDA recall event 29194 · Class II · American Red Cross Blood Services

Key facts

Event ID 29194
Recall numbers B-1540-4, B-1541-4
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, collected from an ineligible donor due to use of the drug Proscar, were distributed.
Initiation date Dec 17, 2003
Termination date Jul 12, 2004
City Cleveland
Country United States
FEI number 1573019

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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