Ideal Eyes 0502539030Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 07613327059427), received between Jun 28, 2021 and Oct 10, 2022 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Optical Problem” (3 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 10, 2022Poor Quality Image; Optical Problem; Optical Problem

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 15571483 ↗
• MalfunctionJun 29, 2021Optical Problem; Poor Quality Image; Optical Problem

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 12084329 ↗
• MalfunctionJun 28, 2021Optical Problem; Poor Quality Image; Optical Problem

  IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

  Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

  MAUDE report 12076694 ↗