Drug recall

Source Plasma

FDA recall event 83450 · Class III · CSL Plasma, Inc.

Key facts

Event ID 83450
Recall numbers B-0822-2019
Recalling firm CSL Plasma, Inc.
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 Jun 20, 2019
Report date Aug 28, 2019
Termination date Aug 19, 2019
City Oak Park
State MI
Country United States
FEI number 1876550

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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