Drug recall

Source Plasma

FDA recall event 72033 · Class II · BPL PLasma, Inc.

Key facts

Event ID 72033
Recall numbers B-0031-16
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 a donor who was previously deferred, were distributed.
Initiation date Feb 19, 2015
Report date Oct 7, 2015
Termination date Oct 1, 2015
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.

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:

Browse all FDA drug and product recalls