Drug recall

Recovered Plasma

FDA recall event 33302 · Class III · Inland Northwest Blood Center

Key facts

Event ID 33302
Recall numbers B-0557-6
Recalling firm Inland Northwest Blood Center
Product type Biologics
Products Recovered Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor for whom donor suitability was not adequately determined, was distributed.
Initiation date Feb 18, 2004
Termination date Jan 26, 2006
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.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

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

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