Drug recall

Source Plasma

FDA recall event 54967 · Class II · CSL Plasma, Inc.

Key facts

Event ID 54967
Recall numbers B-0658-13
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 who was permanently deferred, were distributed.
Initiation date Feb 11, 2010
Report date Feb 6, 2013
Termination date Jan 28, 2013
City Spokane
State WA
Country United States
FEI number 3072740

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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