Drug recall

Cornea

FDA recall event 99974 · Class II · Eversight Illinois

Key facts

Event ID 99974
Recall numbers B-0269-2026
Recalling firm Eversight Illinois
Product type Biologics
Products Cornea
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Corneas, recovered from a donor in which donor eligibility was not adequately determined, were distributed.
Initiation date Jul 9, 2025
Report date Oct 7, 2026
Termination date Sep 25, 2026
City Chicago
State IL
Country United States
FEI number 3001451642

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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