Drug recall

Platelets Pheresis Leukocytes Reduced

FDA recall event 38737 · Class II · Heartland Blood Centers

Key facts

Event ID 38737
Recall numbers B-1534-07
Recalling firm Heartland Blood Centers
Product type Biologics
Products Platelets Pheresis Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, possibly contaminated with air, were distributed.
Initiation date Mar 21, 2007
Termination date Sep 6, 2007
City Aurora
State IL
Country United States
FEI number 1470274

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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