Drug recall

Source Plasma

FDA recall event 70769 · Class II · BPL Plasma, Inc.

Key facts

Event ID 70769
Recall numbers B-0569-15
Recalling firm BPL 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 had been incarcerated, were distributed.
Initiation date Jan 12, 2015
Report date May 6, 2015
Termination date Apr 24, 2015
City Temple Terrace
State FL
Country United States
FEI number 3004158206

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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