Drug recall

Platelets, Pheresis, Leukocytes Reduced

FDA recall event 35338 · Class II · Central Indiana Regional Blood Center, Inc

Key facts

Event ID 35338
Recall numbers B-1840-6
Recalling firm Central Indiana Regional Blood Center, Inc
Product type Biologics
Products Platelets, Pheresis, Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Platelets, which were possibly contaminated with Corynebacterium species, was distributed.
Initiation date Mar 9, 2006
Termination date Sep 18, 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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