Drug recall

Source Plasma

FDA recall event 83124 · Class III · BPL Plasma, Inc.

Key facts

Event ID 83124
Recall numbers B-0696-2019
Recalling firm BPL Plasma, Inc.
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Source Plasma, collected from an ineligible donor, was distributed.
Initiation date Feb 13, 2019
Report date Jun 26, 2019
Termination date Jun 20, 2019
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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