Ideal Eyes 0502539010Recalls & 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
- 7
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 07613327059403), received between May 14, 2019 and Dec 21, 2022 — classified as 7 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (5 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
Device problems
- Poor Quality Image5
- Image Display Error/Artifact2
- Optical Problem2
- Break1
- Moisture Damage1
- Optical Distortion1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Insufficient Information3
- No Known Impact Or Consequence To Patient3
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 21, 2022Optical Distortion; Poor Quality Image; Optical Distortion
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16030490 ↗MalfunctionNov 18, 2021Image Display Error/Artifact; Moisture Damage; Moisture Damage
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 12839001 ↗MalfunctionMay 18, 2021Poor Quality Image; Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11843382 ↗MalfunctionJan 5, 2021Poor Quality Image; Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS A BLURRY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11118848 ↗MalfunctionOct 31, 2019Break; Poor Quality Image; Break
IT WAS REPORTED THAT THE FAILURE MODE WAS RELATED TO INTERNAL MOISTURE AND THE MOISTURE COULD NOT BE WIPED FROM THE SCOPE CAUSING AN UNCLEAR IMAGE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9261075 ↗MalfunctionAug 1, 2019Poor Quality Image
IT WAS REPORTED SCOPE WAS BLURRY DURING PROCEDURE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8850960 ↗MalfunctionMay 14, 2019Image Display Error/Artifact
IT WAS REPORTED THE SCOPE HAD A CLOUDY IMAGE DURING USE, PROCEDURE COMPLETED SUCCESSFULLY WITH A REPLACEMENT SCOPE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8608027 ↗
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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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