Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 71808 · Class III · OneBlood, Inc.

Key facts

Event ID 71808
Recall numbers B-0878-15, B-0879-15
Recalling firm OneBlood, Inc.
Product type Biologics
Products Blood and Blood Products for Reprocessing, Fresh Frozen Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which were labeled with the incorrect product type, were distributed.
Initiation date Jun 12, 2015
Report date Sep 2, 2015
Termination date Aug 21, 2015
City Orlando
State FL
Country United States
FEI number 1072425

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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