Drug recall

Recovered Plasma

FDA recall event 32050 · Class II · American Red Cross Blood Services

Key facts

Event ID 32050
Recall numbers B-1389-5
Recalling firm American Red Cross Blood Services
Product type Biologics
Products Recovered Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, which tested negative for hepatitis, but was collected from an ineligible donor due to a history of jaundice with mononucleosis, was distributed.
Initiation date Oct 15, 2004
Termination date Jun 23, 2005
City Columbus
Country United States
FEI number 1573013

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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