Drug recall

Fresh Frozen Plasma

FDA recall event 30700 · Class III · Inland Northwest Blood Center

Key facts

Event ID 30700
Recall numbers B-0539-5
Recalling firm Inland Northwest Blood Center
Product type Biologics
Products Fresh Frozen Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, manufactured in expired processing bags, were distributed.
Initiation date Jul 21, 2003
Termination date Jan 31, 2005
City Spokane
Country United States
FEI number 3071345

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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