Drug recall

Source Plasma

FDA recall event 32634 · Class II · BioLife Plasma Services LP

Key facts

Event ID 32634
Recall numbers B-0562-6
Recalling firm BioLife Plasma Services LP
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Source Plasma, collected from a previously deferred donor, was distributed.
Initiation date Apr 29, 2004
Termination date Feb 23, 2006
City Hattiesburg
Country United States
FEI number 1076366

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.

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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