Drug recall

Platelets Pheresis Leukocytes Reduced

FDA recall event 38790 · Class II · Community Blood Center

Key facts

Event ID 38790
Recall numbers B-2126-12
Recalling firm Community Blood Center
Product type Biologics
Products Platelets Pheresis Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, with a low platelet count, was distributed.
Initiation date May 5, 2007
Report date Aug 8, 2012
Termination date Aug 1, 2012
City Dayton
State OH
Country United States
FEI number 1570984

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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