Drug recall

Recovered Plasma

FDA recall event 48917 · Class III · Michigan Community Blood Center

Key facts

Event ID 48917
Recall numbers B-1927-08, B-1928-08
Recalling firm Michigan Community Blood Center
Product type Biologics
Products Recovered Plasma, Red blood cells, leukocytes reduced.
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, collected from a donor who received a bone graft within one year of donation, was distributed.
Initiation date Jun 24, 2008
Termination date Aug 29, 2008
City Traverse City
State MI
Country United States
FEI number 1000517886

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.

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

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