Drug recall

Platelets

FDA recall event 30437 · Class II · Carter BloodCare

Key facts

Event ID 30437
Recall numbers B-0324-5
Recalling firm Carter BloodCare
Product type Biologics
Products Platelets
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, that tested reactive for the antibody to hepatitis B core antigen (anti-HBc), was distributed.
Initiation date Dec 18, 2003
Termination date Dec 16, 2004
City Bedford
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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