Drug recall

Source Plasma

FDA recall event 85587 · Class II · CSL Plasma, Inc.

Key facts

Event ID 85587
Recall numbers B-0477-2020
Recalling firm CSL Plasma, Inc.
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Source Plasma, associated with a device collection unexpected event, was distributed.
Initiation date Oct 23, 2019
Report date May 13, 2020
Termination date May 1, 2020
City Highland Park
State MI
Country United States
FEI number 3011534481

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 · Source date:

Browse all FDA drug and product recalls