Drug recall

Source Plasma

FDA recall event 73927 · Class II · BPL Plasma, Inc.

Key facts

Event ID 73927
Recall numbers B-0527-16
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 an ineligible donor, were distributed.
Initiation date Mar 21, 2016
Report date May 25, 2016
Termination date May 17, 2016
City Jacksonville
State FL
Country United States
FEI number 3007895922

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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