Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 67143 · Class II, Class III · Carter BloodCare

Key facts

Event ID 67143
Recall numbers B-0324-14, B-0325-14
Recalling firm Carter BloodCare
Product type Biologics
Products Blood and Blood Products for Reprocessing, Red Blood Cells Leukocytes Reduced
Classification Class II, Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor for whom donor suitability was not adequately determined, were distributed.
Initiation date Dec 16, 2013
Report date Feb 12, 2014
Termination date Jan 31, 2014
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.

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

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