Drug recall

Plasma Frozen, Cryo Reduced

FDA recall event 91430 · Class II · Versiti Indiana Inc

Key facts

Event ID 91430
Recall numbers B-0123-2023
Recalling firm Versiti Indiana Inc
Product type Biologics
Products Plasma Frozen, Cryo Reduced
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Plasma Frozen, Cryo Reduced, which was labeled as Fresh Frozen Plasma, was distributed.
Initiation date Oct 13, 2022
Report date Jan 18, 2023
Termination date Jan 12, 2023
City Indianapolis
State IN
Country United States
FEI number 1873403

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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