Drug recall

Source Plasma

FDA recall event 83694 · Class II · BPL Plasma, Inc.

Key facts

Event ID 83694
Recall numbers B-0898-2019
Recalling firm BPL Plasma, Inc.
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Source Plasma, collected from a donor who received a tattoo within one year of donation, was distributed.
Initiation date Jul 26, 2019
Report date Oct 2, 2019
Termination date Sep 20, 2019
City Lewiston
State ME
Country United States
FEI number 1000514070

At a glance

  • 1–9 Products in this recall
  • 10–99 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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