Drug recall

Platelet Pheresis, Leukocytes Reduced

FDA recall event 31531 · Class II · Central Blood Bank

Key facts

Event ID 31531
Recall numbers B-1001-5
Recalling firm Central Blood Bank
Product type Biologics
Products Platelet Pheresis, Leukocytes Reduced
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Platelet Pheresis, possibly contaminated with bacteria, was distributed.
Initiation date Jan 4, 2005
City Pittsburgh
Country United States
FEI number 2571073

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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