Drug recall

Source Plasma

FDA recall event 85877 · Class III · BPL Plasma Inc.

Key facts

Event ID 85877
Recall numbers B-0591-2020
Recalling firm BPL Plasma Inc.
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Source Plasma products, which may have been exposed to unacceptable temperatures, were distributed.
Initiation date Apr 30, 2020
Report date Jul 29, 2020
Termination date Jul 22, 2020
City Gainesville
State FL
Country United States
FEI number 1052135

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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