Drug recall

Red Blood Cells (Apheresis)

FDA recall event 65053 · Class II · Central Blood Bank

Key facts

Event ID 65053
Recall numbers B-1760-13
Recalling firm Central Blood Bank
Product type Biologics
Products Red Blood Cells (Apheresis)
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood products, which did not undergo the required quality control testing, were distributed.
Initiation date Feb 19, 2013
Report date Jun 5, 2013
Termination date May 24, 2013
City Pittsburgh
State PA
Country United States
FEI number 2571073

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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