Drug recall

Platelets Pheresis Leukocytes Reduced

FDA recall event 68869 · Class II · LifeServe Blood Center

Key facts

Event ID 68869
Recall numbers B-0882-14
Recalling firm LifeServe 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 for which some quality control procedures were not performed, was distributed.
Initiation date Jun 12, 2014
Report date Aug 13, 2014
Termination date Aug 5, 2014
City Des Moines
State IA
Country United States
FEI number 1970355

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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