Drug recall

Source Plasma

FDA recall event 27895 · Class II · Alpha Therapeutic Corporation

Key facts

Event ID 27895
Recall numbers B-1840-4
Recalling firm Alpha Therapeutic Corporation
Product type Biologics
Products Source Plasma
Classification Class II
Status Completed
Voluntary or mandated Firm Initiated
Reason for recall Blood products, that tested negative for viral markers, but were collected from an ineligible donor due to intravenous (IV) drug use, were distributed.
Initiation date May 13, 2002
City Bakersfield
Country United States
FEI number 2077772

At a glance

  • 1–9 Products in this recall
  • 1–9 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