Drug recall

Recovered Plasma

FDA recall event 30796 · Class II · Inland Northwest Blood Center

Key facts

Event ID 30796
Recall numbers B-0545-5
Recalling firm Inland Northwest Blood Center
Product type Biologics
Products Recovered Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from an ineligible donor due to previous blood product administration, was distributed.
Initiation date Jul 21, 2003
Termination date Feb 22, 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.

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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