Drug recall

Fresh Frozen Plasma Pheresis

FDA recall event 35972 · Class III · Gulf Coast Regional Blood Center

Key facts

Event ID 35972
Recall numbers B-1448-6
Recalling firm Gulf Coast Regional Blood Center
Product type Biologics
Products Fresh Frozen Plasma Pheresis
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, which lacked assurance of proper shipping temperatures, was distributed.
Initiation date Oct 19, 2005
Termination date Sep 22, 2006
City Houston
Country United States
FEI number 3002133806

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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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports

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