Drug recall

Source Plasma

FDA recall event 56469 · Class II · CSL Plasma, Inc.

Key facts

Event ID 56469
Recall numbers B-2352-12
Recalling firm CSL Plasma, Inc.
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor, whose suitability to donate was not adequately determined, was distributed.
Initiation date Jul 30, 2010
Report date Aug 15, 2012
Termination date Aug 6, 2012
City Hamilton
State OH
Country United States
FEI number 3005600077

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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