Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 89261 · Class III · American National Red Cross

Key facts

Event ID 89261
Recall numbers B-0159-2022
Recalling firm American National Red Cross
Product type Biologics
Products Blood and Blood Products for Reprocessing
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Blood and Blood Products for Reprocessing, for which donor eligibility screening was incomplete, were distributed.
Initiation date Nov 18, 2021
Report date Jan 26, 2022
Termination date Jan 18, 2022
City Portland
State OR
Country United States
FEI number 3072996

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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