Drug recall

Source Plasma

FDA recall event 82834 · Class III · CSL Plasma, Inc

Key facts

Event ID 82834
Recall numbers B-0596-2019
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 blood products, collected from a donor who was illiterate, were distributed.
Initiation date Mar 22, 2019
Report date Jun 19, 2019
Termination date Jun 11, 2019
City Westwego
State LA
Country United States
FEI number 3012118618

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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