Drug recall

Source Plasma

FDA recall event 28837 · Class II · BioLife Plasma Services, Lp

Key facts

Event ID 28837
Recall numbers B-1298-4
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 Blood products, collected from an unsuitable donor based on previous deferral for IV drug use, were distributed.
Initiation date Apr 17, 2001
Termination date Jun 4, 2004
City Odessa
Country United States
FEI number 1643464

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

Browse all FDA drug and product recalls