Drug recall

Platelets

FDA recall event 41131 · Class II · Our Lady Of The Lake Hospital Inc

Key facts

Event ID 41131
Recall numbers B-1781-08
Recalling firm Our Lady Of The Lake Hospital Inc
Product type Biologics
Products Platelets
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who had taken aspirin, were distributed.
Initiation date Dec 1, 2005
Termination date Aug 14, 2008
City Baton Rouge
State LA
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.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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