Drug recall

Source Plasma

FDA recall event 69711 · Class III · Octapharma Plasma, Inc.

Key facts

Event ID 69711
Recall numbers B-0171-15
Recalling firm Octapharma Plasma, Inc.
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who should have been deferred due to history, were distributed.
Initiation date Oct 8, 2014
Report date Nov 26, 2014
Termination date Nov 20, 2014
City Charlotte
State NC
Country United States
FEI number 1071676

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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