Drug recall

Source Plasma

FDA recall event 85666 · Class III · CSL Plasma Inc

Key facts

Event ID 85666
Recall numbers B-0498-2020
Recalling firm CSL Plasma Inc
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Source Plasma units, collected from a donor whose donor eligibility was incomplete, were distributed.
Initiation date Feb 4, 2020
Report date May 27, 2020
Termination date May 15, 2020
City Houston
State TX
Country United States
FEI number 3014277827

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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