Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 76530 · Class II · Inland Northwest Blood Center

Key facts

Event ID 76530
Recall numbers B-0449-2017
Recalling firm Inland Northwest Blood Center
Product type Biologics
Products Blood and Blood Products for Reprocessing
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from an ineligible donor, was distributed.
Initiation date Jan 17, 2017
Report date Apr 5, 2017
Termination date Mar 29, 2017
City Spokane
State WA
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 · Source date:

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