Drug recall

Source Plasma

FDA recall event 85672 · Class III · CSL Plasma, Inc.

Key facts

Event ID 85672
Recall numbers B-0508-2020
Recalling firm CSL Plasma, Inc.
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Source Plasma units, collected from a donor whose donor screening record was either incomplete or incorrect, were distributed.
Initiation date Mar 4, 2020
Report date May 27, 2020
Termination date May 15, 2020
City Jackson
State MI
Country United States
FEI number 3014947859

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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