Drug recall

Blood Products - Other

FDA recall event 91627 · Class III · Versiti Illinois Inc

Key facts

Event ID 91627
Recall numbers B-0190-2023
Recalling firm Versiti Illinois Inc
Product type Biologics
Products Blood Products - Other
Classification Class III
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Blood Product, returned to the blood center without confirmation that the product had been stored properly, was distributed.
Initiation date May 27, 2022
Report date Feb 22, 2023
Termination date Feb 13, 2023
City Aurora
State IL
Country United States
FEI number 1470274

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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