Drug recall

Source Plasma

FDA recall event 53632 · Class II · CSL Plasma, Inc.

Key facts

Event ID 53632
Recall numbers B-2549-12
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 scheduled physical examination was incomplete, were distributed.
Initiation date Aug 31, 2009
Report date Sep 26, 2012
Termination date Sep 17, 2012
City Racine
State WI
Country United States
FEI number 2129805

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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