Drug recall

Source Plasma

FDA recall event 84476 · Class III · CSL Plasma

Key facts

Event ID 84476
Recall numbers B-0202-2020
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 Racine
State WI
Country United States
FEI number 2129805

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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