Drug recall

Source plasma

FDA recall event 27610 · Class II · ZLB Bioplasma, Inc.

Key facts

Event ID 27610
Recall numbers B-0328-4
Recalling firm ZLB Bioplasma, 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 in which the questions regarding Creutzfeldt-Jakob disease (CJD) were incomplete on the donation record, were distributed.
Initiation date Feb 21, 2003
City Oak Park
Country United States
FEI number 1876550

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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