Drug recall

Platelets

FDA recall event 26554 · Class II · Our Lady of the Lake Regional Medical Center Blood Bank

Key facts

Event ID 26554
Recall numbers B-1432-3
Recalling firm Our Lady of the Lake Regional Medical Center Blood Bank
Product type Biologics
Products Platelets
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from an unsuitable donor based on travel to an area considered endemic for malaria, was distributed.
Initiation date Oct 3, 2001
City Baton Rouge
Country United States
FEI number 2370424

At a glance

  • 1–9 Products in this recall
  • None 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