Drug recall

Cryoprecipitated AHF

FDA recall event 26802 · Class II · American Red Cross Blood Services

Key facts

Event ID 26802
Recall numbers B-1711-3, B-1712-3, B-1713-3, B-1714-3
Recalling firm American Red Cross Blood Services
Product type Biologics
Products Cryoprecipitated AHF, Fresh Frozen Plasma, Recovered Plasma, Red Blood Cells, Leukocytes Reduced
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which tested negative for hepatitis but were collected from a donor who subsequently tested positive for an unknown type of hepatitis, were distributed.
Initiation date Mar 21, 2003
City Johnstown
Country United States
FEI number 2573016

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