Drug recall

Source Plasma

FDA recall event 32696 · Class II · Aventis Bio-Services Inc

Key facts

Event ID 32696
Recall numbers B-1895-5
Recalling firm Aventis Bio-Services Inc
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Source Plasma, collected from a donor who had received a piercing within 12 months of donation, was distributed.
Initiation date Nov 22, 2002
Termination date Aug 25, 2005
City Kansas City
Country United States
FEI number 1930460

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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