Drug recall

Source Plasma

FDA recall event 71439 · Class II · CSL Plasma, Inc

Key facts

Event ID 71439
Recall numbers B-0728-15
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 did not have a complete physical examination, were distributed.
Initiation date Apr 7, 2015
Report date Jul 8, 2015
Termination date Jul 2, 2015
City Gulfport
State MS
Country United States
FEI number 3010978848

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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