Drug recall

Source Plasma

FDA recall event 81827 · Class III · CSL Plasma Inc

Key facts

Event ID 81827
Recall numbers B-0271-2019
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 Sep 25, 2018
Report date Feb 13, 2019
Termination date Feb 7, 2019
City Jonesboro
State GA
Country United States
FEI number 3010854409

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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