Drug recall

Fresh Frozen Plasma

FDA recall event 67220 · Class II · Michigan Blood

Key facts

Event ID 67220
Recall numbers B-0349-14
Recalling firm Michigan Blood
Product type Biologics
Products Fresh Frozen Plasma
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor considered to be at increased risk for variant Creutzfeldt-Jakob Disease (vCJD), was distributed.
Initiation date Nov 25, 2013
Report date Feb 12, 2014
Termination date Feb 5, 2014
City Grand Rapids
State MI
Country United States
FEI number 1875548

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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