Drug recall

Human Cornea

FDA recall event 83262 · Class II · Eversight Illinois (Chicago)

Key facts

Event ID 83262
Recall numbers B-0753-2019
Recalling firm Eversight Illinois (Chicago)
Product type Biologics
Products Human Cornea
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall Human corneas, recovered from a donor whose donor eligibility determination failed to ensure that the donor was free from risk factors for, and clinical evidence of infection due to relevant…
Initiation date Jun 26, 2019
Report date Jul 10, 2019
Termination date Jul 3, 2019
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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