Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 63757 · Class II · Carter BloodCare

Key facts

Event ID 63757
Recall numbers B-0593-13, B-0594-13
Recalling firm Carter BloodCare
Product type Biologics
Products Blood and Blood Products for Reprocessing, Red Blood Cells Leukocytes Reduced
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor who was previously deferred, were distributed
Initiation date Nov 9, 2012
Report date Jan 2, 2013
Termination date Dec 27, 2012
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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