Drug recall

Recovered Plasma

FDA recall event 34209 · Class II · American National Red Cross, The

Key facts

Event ID 34209
Recall numbers B-0593-6, B-0594-6
Recalling firm American National Red Cross, The
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 a donor with a history of hepatitis A, were distributed., Blood products, which tested negative for hepatitis, were collected from a donor with a history of hepatitis A, were distributed.
Initiation date May 22, 2003
Termination date Feb 15, 2006
City Pomona
Country United States
FEI number 2072994

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

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

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