Drug recall

Source Plasma

FDA recall event 27576 · Class III · ZLB Plasma Services

Key facts

Event ID 27576
Recall numbers B-0345-4
Recalling firm ZLB Plasma Services
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor whose medical history screening did not include questioning regarding risk factors for new variant Creutizfeldt-Jacob disease (nvCJD), were distributed.
Initiation date Jun 2, 2003
Termination date Feb 6, 2004
City Columbus
Country United States
FEI number 1572439

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

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