Drug recall

Platelets

FDA recall event 38735 · Class II · Michigan Community Blood Centers

Key facts

Event ID 38735
Recall numbers B-0478-08
Recalling firm Michigan Community Blood Centers
Product type Biologics
Products Platelets
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, which was manufactured from a whole blood unit in which an associated blood component contained clots, was distributed.
Initiation date Mar 13, 2007
Termination date Dec 6, 2007
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.

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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