Drug recall

Platelets

FDA recall event 33123 · Class II, Class III · Gulf Coast Regional Blood Center

Key facts

Event ID 33123
Recall numbers B-2215-5, B-2216-5, B-2217-5
Recalling firm Gulf Coast Regional Blood Center
Product type Biologics
Products Platelets, Recovered Plasma, Red Blood Cells, Leukocytes Reduced
Classification Class II, Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from an ineligible donor, were distributed.
Initiation date Jul 12, 2004
Termination date Oct 21, 2005
City Houston
Country United States
FEI number 3002133806

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