Drug recall

Source Plasma

FDA recall event 25671 · Class II · Aventis Bio-Services Inc

Key facts

Event ID 25671
Recall numbers B-0769-3
Recalling firm Aventis Bio-Services Inc
Product type Biologics
Products Source Plasma
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which were collected from a donor who tested positive for HIV and hepatitis prior to donation, were shipped.
Initiation date Jan 7, 2003
City Knoxville
Country United States

At a glance

  • 1–9 Products in this recall

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