Drug recall

source plasma

FDA recall event 26569 · Class II · Bio-Blood Components, Inc.

Key facts

Event ID 26569
Recall numbers B-1469-3
Recalling firm Bio-Blood Components, Inc.
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 who had body piercing within twelve months of donation, was distributed.
Initiation date Apr 28, 2003
City Muskegon
Country United States
FEI number 1000115480

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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