Drug recall

Source Plasma

FDA recall event 82575 · Class III · CSL PLASMA, INC

Key facts

Event ID 82575
Recall numbers B-0491-2019
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 for whom donor suitability was not adequately determined, was distributed.
Initiation date Feb 28, 2019
Report date Apr 24, 2019
Termination date Apr 12, 2019
City Philadelphia
State PA
Country United States
FEI number 3011813573

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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