Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 80395 · Class III · American Red Cross Blood Services

Key facts

Event ID 80395
Recall numbers B-0691-2018
Recalling firm American Red Cross Blood Services
Product type Biologics
Products Blood and Blood Products for Reprocessing
Classification Class III
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Blood product, for which donor screening was inadequately performed, was distributed.
Initiation date May 26, 2018
Report date Aug 1, 2018
Termination date Jul 24, 2018
City Birmingham
State AL
Country United States
FEI number 1073001

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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