Drug recall

Platelets Pheresis

FDA recall event 28606 · Class II · Central Texas Regional Blood & Tissue Center

Key facts

Event ID 28606
Recall numbers B-1126-4
Recalling firm Central Texas Regional Blood & Tissue Center
Product type Biologics
Products Platelets Pheresis
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from an ineligible donor due to use of the drug Proscar, was distributed.
Initiation date Jul 12, 2001
Termination date Apr 22, 2004
City Austin
Country United States
FEI number 1671794

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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