Drug recall

Source Plasma

FDA recall event 35734 · Class II · BioLife Plasma Services, L.P.

Key facts

Event ID 35734
Recall numbers B-0329-7
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 received a tattoo and piercing within 12 months of donation, were distributed.
Initiation date May 10, 2006
Termination date Nov 21, 2006
City Fort Wayne
Country United States
FEI number 1876564

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