Drug recall

Source Plasma

FDA recall event 31552 · Class II · Aventis Bio-Services, Inc

Key facts

Event ID 31552
Recall numbers B-1042-5
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 not tested for syphilis, were distributed.
Initiation date Feb 6, 2002
City San Angelo
Country United States
FEI number 1000306162

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