Drug recall

Fresh Frozen Plasma

FDA recall event 33099 · Class III · Carter BloodCare

Key facts

Event ID 33099
Recall numbers B-2180-5, B-2181-5, B-2182-5, B-2183-5, B-2184-5
Recalling firm Carter BloodCare
Product type Biologics
Products Fresh Frozen Plasma, Platelets, Recovered Plasma, Red Blood Cells, Red Blood Cells, Leukocytes Reduced
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from an unsuitable donor, were distributed.
Initiation date Jan 10, 2005
Termination date Oct 3, 2005
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.

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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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