Drug recall

Fresh Frozen Plasma Pheresis

FDA recall event 37208 · Class II · American National Red Cross (The) - North Central Region

Key facts

Event ID 37208
Recall numbers B-0890-07, B-0891-07
Recalling firm American National Red Cross (The) - North Central Region
Product type Biologics
Products Fresh Frozen Plasma Pheresis, Platelets Pheresis, Leukocytes Reduced, Irradiated
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, associated with a unit of platelets that was possibly contaminated with Staphylococcus aureus, were distributed.
Initiation date Nov 4, 2003
Termination date Mar 22, 2007
City Saint Paul
Country United States
FEI number 2173038

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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