Drug recall

Plasma

FDA recall event 35925 · Class III · American Natl Red Cross Mid At

Key facts

Event ID 35925
Recall numbers B-0217-7, B-0218-7
Recalling firm American Natl Red Cross Mid At
Product type Biologics
Products Plasma, Red Blood Cells, Leukocytes Reduced Unit (1 unit) 29KH41430
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from an ineligible donor, were distributed.
Initiation date May 23, 2005
Termination date Nov 14, 2006
City Norfolk
Country United States
FEI number 1173024

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

Browse all FDA drug and product recalls