Drug recall

Fresh Frozen Plasma

FDA recall event 26088 · Class II · Carter BloodCare

Key facts

Event ID 26088
Recall numbers B-1010-3, B-1011-3, B-1012-3
Recalling firm Carter BloodCare
Product type Biologics
Products Fresh Frozen Plasma, Platelets, Red Blood Cells
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor whose body temperature was not determined, were distributed.
Initiation date Jul 3, 2001
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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