Drug recall

Platelets, Pathogen Reduced

FDA recall event 89709 · Class III · ARUP Laboratories, Inc.

Key facts

Event ID 89709
Recall numbers B-0275-2022
Recalling firm ARUP Laboratories, Inc.
Product type Biologics
Products Platelets, Pathogen Reduced
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Misbranded platelet product was distributed.
Initiation date Jan 21, 2022
Report date Mar 30, 2022
Termination date Mar 18, 2022
City Sandy
State UT
Country United States
FEI number 1720911

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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