Drug recall

Platelets

FDA recall event 33612 · Class II · Gulf Coast Regional Blood Center

Key facts

Event ID 33612
Recall numbers B-0226-6
Recalling firm Gulf Coast Regional Blood Center
Product type Biologics
Products Platelets
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which were made from whole blood units that did not meet appropriate temperatures for platelet manufacture, were distributed.
Initiation date Jun 17, 2004
Termination date Dec 2, 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

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