Drug recall

Platelets

FDA recall event 27569 · Class II · HCSC Blood Center

Key facts

Event ID 27569
Recall numbers B-0464-4
Recalling firm HCSC Blood Center
Product type Biologics
Products Platelets
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Platelets, manufactured with an incorrect centrifuge setting, were distributed.
Initiation date Sep 11, 2002
Termination date Jan 30, 2004
City Bethlehem
Country United States
FEI number 2573135

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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