Drug recall

Red Blood Cells

FDA recall event 28543 · Class II · Blood Center The

Key facts

Event ID 28543
Recall numbers B-1223-4
Recalling firm Blood Center The
Product type Biologics
Products Red Blood Cells
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, corresponding to a unit of Platelets that was pooled and was possibly contaminated with Staphylococcus sp. bacteria, was distributed.
Initiation date Aug 18, 2003
Termination date May 21, 2004
City New Orleans
Country United States
FEI number 2374536

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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