Ideal Eyes 0502859030Recalls & reported problems
Stryker Corporation · Laparoscope, Autoclavable, Full Screen, 30 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
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 07613327060171), received between Aug 12, 2020 and Feb 21, 2025 — classified as 4 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.
Reports received per month
Most reported problems
Device problems
- Optical Problem3
- Poor Quality Image3
- Fogging1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Menorrhagia1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 21, 2025Fogging; Optical Problem; Fogging; Optical Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21433307 ↗MalfunctionSep 12, 2023Poor Quality Image; Optical Problem; Poor Quality Image; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17733583 ↗MalfunctionJun 28, 2021Poor Quality Image; Optical Problem; Poor Quality Image; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: Menorrhagia; No Clinical Signs, Symptoms or Conditions
MAUDE report 12076668 ↗MalfunctionAug 12, 2020Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS A BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions; No Known Impact Or Consequence To Patient
MAUDE report 10396055 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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