Drug recall

Red Blood Cells

FDA recall event 31977 · Class II · Heartland Blood Centers

Key facts

Event ID 31977
Recall numbers B-1326-5
Recalling firm Heartland Blood Centers
Product type Biologics
Products Red Blood Cells
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed.
Initiation date Apr 4, 2005
Termination date Jun 3, 2005
City Aurora
Country United States
FEI number 1470274

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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