Drug recall

Platelets Pheresis

FDA recall event 33461 · Class II · Belle Bonfils Memorial Blood Center

Key facts

Event ID 33461
Recall numbers B-0148-6
Recalling firm Belle Bonfils Memorial Blood Center
Product type Biologics
Products Platelets Pheresis
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which tested negative for the cytomegalovirus (CMV) but were collected from a donor who previously tested positive for CMV, were distributed.
Initiation date Dec 1, 1997
Termination date Nov 16, 2005
City Denver
Country United States
FEI number 3000210247

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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