Drug recall

Cornea

FDA recall event 91592 · Class II · Eversight Illinois (Chicago)

Key facts

Event ID 91592
Recall numbers B-0195-2023
Recalling firm Eversight Illinois (Chicago)
Product type Biologics
Products Cornea
Classification Class II
Status Terminated
Voluntary or mandated Voluntary: Firm Initiated
Reason for recall Corneas, in which donor testing was conducted with an unacceptable sample, were distributed.
Initiation date May 31, 2022
Report date Feb 22, 2023
Termination date Feb 14, 2023
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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