Drug recall

Source Plasma

FDA recall event 82576 · Class III · CSL Plasma

Key facts

Event ID 82576
Recall numbers B-0492-2019
Recalling firm CSL Plasma
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Source Plasma, collected from a donor who was illiterate, was distributed.
Initiation date Feb 22, 2019
Report date Apr 24, 2019
Termination date Apr 12, 2019
City Fort Gratiot
State MI
Country United States
FEI number 3013154944

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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