Drug recall

Platelets Pheresis Leukocytes Reduced, unit 4728726 (split) (2 units)

FDA recall event 36140 · Class II · Central Indiana Regional Blood Center, Inc

Key facts

Event ID 36140
Recall numbers B-0131-7
Recalling firm Central Indiana Regional Blood Center, Inc
Product type Biologics
Products Platelets Pheresis Leukocytes Reduced, unit 4728726 (split) (2 units)
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which were labeled with the incorrect platelet yield, were distributed.
Initiation date Aug 3, 2006
Termination date Nov 3, 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.

About FDA drug and product recalls

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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