Drug recall

Source Plasma

FDA recall event 72483 · Class II · BPL Plasma

Key facts

Event ID 72483
Recall numbers B-0092-16
Recalling firm BPL Plasma
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor who received a piercing within one year of donation, was distributed.
Initiation date Sep 10, 2015
Report date Nov 25, 2015
Termination date Nov 16, 2015
City Carbondale
State IL
Country United States
FEI number 3001451631

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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