Drug recall

Source Plasma

FDA recall event 86918 · Class III · BPL Plasma, Inc.

Key facts

Event ID 86918
Recall numbers B-0150-2021
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 units, not meeting product specifications, were distributed.
Initiation date Jul 25, 2020
Report date Dec 23, 2020
Termination date Dec 16, 2020
City College Station
State TX
Country United States
FEI number 3000215642

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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