Drug recall

Red Blood Cells, Autologous

FDA recall event 26511 · Class II · WE & Lela I Stewart Blood Center, Inc

Key facts

Event ID 26511
Recall numbers B-1449-3
Recalling firm WE & Lela I Stewart Blood Center, Inc
Product type Biologics
Products Red Blood Cells, Autologous
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Autologous blood products, which tested repeatedly reactive for infectious disease tests, were distributed without the "Biohazard" label on the bag.
Initiation date Mar 14, 2000
City Tyler
Country United States
FEI number 1672331

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

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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