Drug recall

Source plasma

FDA recall event 27222 · Class III · Aventis Bio-Services, Inc.

Key facts

Event ID 27222
Recall numbers B-0031-4
Recalling firm Aventis Bio-Services, Inc.
Product type Biologics
Products Source plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from ineligible donors, were distributed.
Initiation date Mar 23, 2003
Termination date Dec 5, 2003
City Indianapolis
Country United States
FEI number 1876559

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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