Drug recall

Source Plasma

FDA recall event 69991 · Class II · BioLife Plasma Services, L.P.

Key facts

Event ID 69991
Recall numbers B-0328-15
Recalling firm BioLife Plasma Services, L.P.
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor with a history of incarceration, was distributed.
Initiation date Nov 7, 2014
Report date Feb 4, 2015
Termination date Jan 26, 2015
City Broken Arrow
State OK
Country United States
FEI number 3007991124

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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