Drug recall

Fresh Frozen Plasma

FDA recall event 39124 · Class III · Community Blood Center of Greater Kansas City

Key facts

Event ID 39124
Recall numbers B-2310-12, B-2311-12
Recalling firm Community Blood Center of Greater Kansas City
Product type Biologics
Products Fresh Frozen Plasma, Red Blood Cells Leukocytes Reduced
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, for which viral marker testing was incomplete, were distributed.
Initiation date May 2, 2007
Report date Aug 15, 2012
Termination date Aug 6, 2012
City Kansas City
State MO
Country United States
FEI number 1972933

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 · Source date:

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