Drug recall

Platelets Pheresis Leukocytes Reduced

FDA recall event 36447 · Class II · Coastal Bend Blood Center

Key facts

Event ID 36447
Recall numbers B-0292-7, B-0293-7
Recalling firm Coastal Bend Blood Center
Product type Biologics
Products Platelets Pheresis Leukocytes Reduced, Platelets Pheresis Leukocytes Reduced Irradiated
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who had previously donated a syphilis reactive unit, were distributed.
Initiation date May 2, 2005
Termination date Jan 9, 2007
City Corpus Christi
Country United States
FEI number 1671283

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

Browse all FDA drug and product recalls