Drug recall

Source Plasma

FDA recall event 29152 · Class II · Zlb Bioplasma Services

Key facts

Event ID 29152
Recall numbers B-1568-4
Recalling firm Zlb Bioplasma Services
Product type Biologics
Products Source Plasma
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor whose medical history was incomplete, were distributed.
Initiation date Aug 7, 2002
City Boca Raton
Country United States
FEI number 3003507515

At a glance

  • 1–9 Products in this recall
  • None 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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