Drug recall

Source Plasma

FDA recall event 45180 · Class II · BioLife Plasma Services L.P.

Key facts

Event ID 45180
Recall numbers B-2178-13
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 products, collected from a donor who was previously HIV-1/2 reactive, were distributed.
Initiation date Jul 27, 2007
Report date Aug 7, 2013
Termination date Jul 29, 2013
City Van Nuys
State CA
Country United States
FEI number 3005304611

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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