Drug recall

Apheresis Platelets, Leukocytes Reduced, Irradiated

FDA recall event 88790 · Class II · LifeServe Blood Center

Key facts

Event ID 88790
Recall numbers B-0003-2022
Recalling firm LifeServe Blood Center
Product type Biologics
Products Apheresis Platelets, Leukocytes Reduced, Irradiated
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Leukoreduced, Irradiated Apheresis Platelets, for which documentation of irradiation was incomplete, were distributed.
Initiation date Sep 20, 2021
Report date Nov 3, 2021
Termination date Oct 26, 2021
City Des Moines
State IA
Country United States
FEI number 1970355

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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