Drug recall

Source Plasma

FDA recall event 82170 · Class III · Octapharma Plasma Donation Center Aurora

Key facts

Event ID 82170
Recall numbers B-0325-2019
Recalling firm Octapharma Plasma Donation Center Aurora
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Source Plasma units, collected from an ineligible donor, were distributed.
Initiation date Oct 16, 2018
Report date Mar 6, 2019
Termination date Feb 25, 2019
City Aurora
State IL
Country United States
FEI number 3006200209

At a glance

  • 1–9 Products in this recall
  • 1–9 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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