Drug recall

Red Blood Cells, Leukocytes Reduced

FDA recall event 30617 · Class II · South Bend Medical Foundation

Key facts

Event ID 30617
Recall numbers B-0548-5
Recalling firm South Bend Medical Foundation
Product type Biologics
Products Red Blood Cells, Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Red Cells, lacking proper pre-transfusion testing, were distributed.
Initiation date Oct 4, 2004
Termination date Mar 8, 2005
City S Bend
Country United States
FEI number 1870308

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.

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

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