Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 69491 · Class II · OneBlood, Inc.

Key facts

Event ID 69491
Recall numbers B-0109-15
Recalling firm OneBlood, Inc.
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 a donor with a risk factor associated with Creutzfeldt-Jacob Disease, was distributed.
Initiation date Aug 27, 2014
Report date Nov 5, 2014
Termination date Oct 30, 2014
City St Petersburg
State FL
Country United States
FEI number 1070196

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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