Drug recall

Blood and Blood Products for Reprocessing

FDA recall event 88896 · Class III · American Red Cross Blood Services

Key facts

Event ID 88896
Recall numbers B-0029-2022
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 Voluntary: Firm Initiated
Reason for recall Blood products, for which donor eligibility screening was incomplete, were distributed.
Initiation date Jul 30, 2021
Report date Nov 10, 2021
Termination date Nov 4, 2021
City Saint Louis
State MO
Country United States
FEI number 1973035

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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