Drug recall

Source Plasma

FDA recall event 37209 · Class II · BioLife Plasma Services, L.P.

Key facts

Event ID 37209
Recall numbers B-0889-7
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 had received the MMR caccine within two weeks of donation, were distributed.
Initiation date Jun 24, 2003
Termination date Mar 22, 2007
City Bismarck
Country United States
FEI number 3003102460

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.

About FDA drug and product recalls

FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.

Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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