Drug recall

Red Blood Cells

FDA recall event 28735 · Class III · Delta Blood Bank

Key facts

Event ID 28735
Recall numbers B-1247-4
Recalling firm Delta Blood Bank
Product type Biologics
Products Red Blood Cells
Classification Class III
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood Product, collected from a donor whose body temperature was not documented, was distributed.
Initiation date Oct 27, 1998
City Stockton
Country United States
FEI number 2970116

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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