Drug recall

Source Plasma

FDA recall event 84484 · Class III · CSL Plasma

Key facts

Event ID 84484
Recall numbers B-0210-2020
Recalling firm CSL Plasma
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 who was illiterate, was distributed.
Initiation date Sep 30, 2019
Report date Jan 15, 2020
Termination date Jan 8, 2020
City Omaha
State NE
Country United States
FEI number 1978037

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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FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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