Drug recall

Source Plasma

FDA recall event 74852 · Class II · BloodSource, Inc.

Key facts

Event ID 74852
Recall numbers B-0695-16
Recalling firm BloodSource, Inc.
Product type Biologics
Products Source Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor who was allowed to donate without a current physical, was distributed.
Initiation date Jun 27, 2016
Report date Aug 17, 2016
Termination date Aug 10, 2016
City Mather
State CA
Country United States
FEI number 3007101464

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.

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

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