Drug recall

Source Plasma

FDA recall event 32234 · Class III · Biolife Plasma Services L.P.

Key facts

Event ID 32234
Recall numbers B-1657-5
Recalling firm Biolife Plasma Services L.P.
Product type Biologics
Products Source Plasma
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, collected from a donor that did not answer the medical history questions, were distributed.
Initiation date Sep 24, 2001
Termination date Jul 21, 2005
City Ogden
Country United States
FEI number 1770167

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