Drug recall

Source Plasma

FDA recall event 37789 · Class III · Talecris Plasma Resources

Key facts

Event ID 37789
Recall numbers B-1314-07
Recalling firm Talecris Plasma Resources
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from donors who did not have a complete medical history interview, were distributed.
Initiation date Dec 21, 2006
Termination date May 10, 2007
City Peoria
Country United States
FEI number 1000514678

At a glance

  • 1–9 Products in this recall
  • 1–9 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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