Drug recall

Source Plasma

FDA recall event 85046 · Class III · CSL Plasma Inc.

Key facts

Event ID 85046
Recall numbers B-0357-2020
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, collected from a donor whose donor eligibility was incomplete, was distributed.
Initiation date Jan 13, 2020
Report date Mar 4, 2020
Termination date Feb 27, 2020
City Baltimore
State MD
Country United States
FEI number 3012614076

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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