Drug recall

Fresh Frozen Plasma

FDA recall event 30613 · Class II · Central Indiana Regional Blood Center, Inc

Key facts

Event ID 30613
Recall numbers B-0430-5
Recalling firm Central Indiana Regional Blood Center, Inc
Product type Biologics
Products Fresh Frozen Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected by a method that may have compromised the sterility of the product, was distributed.
Initiation date Nov 3, 2004
Termination date Jan 14, 2005
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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