Drug recall

Source Plasma

FDA recall event 82956 · Class II · CSL Plasma Inc

Key facts

Event ID 82956
Recall numbers B-0688-2019
Recalling firm CSL Plasma Inc
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Source Plasma, which may have been contaminated with saline during collection, was distributed.
Initiation date Apr 3, 2019
Report date Jun 26, 2019
Termination date Jun 17, 2019
City El Paso
State TX
Country United States
FEI number 1047112

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.

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Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date:

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