Drug recall

Source Plasma

FDA recall event 81257 · Class III · CSL Plasma, Inc

Key facts

Event ID 81257
Recall numbers B-0044-2019
Recalling firm CSL Plasma, Inc
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from an ineligible donor, were distributed.
Initiation date Jul 19, 2018
Report date Oct 31, 2018
Termination date Oct 22, 2018
City San Antonio
State TX
Country United States
FEI number 1626759

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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