Drug recall

Source Plasma

FDA recall event 42958 · Class III · CSL Plasma

Key facts

Event ID 42958
Recall numbers B-0213-15
Recalling firm CSL Plasma
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who was previously deferred for unsuitable test results, were distributed.
Initiation date Aug 10, 2006
Report date Dec 17, 2014
Termination date Dec 5, 2014
City Springfield
State OH
Country United States
FEI number 1527870

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.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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