Drug recall

Platelets Pheresis Leukocytes Reduced

FDA recall event 35363 · Class III · Central Indiana Regional Blood Center, Inc

Key facts

Event ID 35363
Recall numbers B-1414-6
Recalling firm Central Indiana Regional Blood Center, Inc
Product type Biologics
Products Platelets Pheresis Leukocytes Reduced
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which were not manufactured in accordance to acceptable product specifications, were distributed.
Initiation date Apr 19, 2006
Termination date Jul 11, 2006
City Indianapolis
Country United States
FEI number 1873403

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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