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Ideal Eyes 0502859010Recalls & reported problems

Stryker Corporation · Laparoscope, Autoclavable, Full Screen, 0 DEG View Direction. · Class 2

All models of Ideal Eyes (9)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327060294), received between Feb 4, 2020 and Feb 4, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Moisture or Humidity Problem” (1 report).

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

Device problems

  • Moisture or Humidity Problem1
  • Optical Problem1
  • Poor Quality Image1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 4, 2020Poor Quality Image; Moisture or Humidity Problem; Optical Problem; Optical Problem

    IT WAS REPORTED THAT THE MOISTURE COULD NOT BE WIPED FROM THE SCOPE. FILE MALFUNCTION DUE TO UNCLEAR IMAGE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9665246 ↗

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Sources and updates

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