Drug recall

Recovered Plasma

FDA recall event 40354 · Class II, Class III · Carter BloodCare

Key facts

Event ID 40354
Recall numbers B-0471-08, B-0472-08
Recalling firm Carter BloodCare
Product type Biologics
Products Recovered Plasma, Red Blood Cells Leukocytes Reduced Irradiated
Classification Class II, Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who had a rash, were distributed.
Initiation date Jun 15, 2005
Termination date Dec 11, 2007
City Bedford
State TX
Country United States
FEI number 3002603147

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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