Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 68822 · Class II · Indiana Blood Center

Key facts

Event ID 68822
Recall numbers B-0862-14
Recalling firm Indiana 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 products, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), were distributed.
Initiation date Jun 27, 2014
Report date Aug 27, 2014
Termination date Aug 19, 2014
City Indianapolis
State IN
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 · Source date:

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