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Precision Ideal Eyes 0502103030Recalls & reported problems

Stryker Corporation · HD Laparoscope, Autoclavable, 30 DEG View Direction · Class 2

All models of Precision Ideal Eyes (10)

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

Quick summary

This Stryker Precision Ideal Eyes laparoscope is an HD scope used in general and plastic surgery. Reports mostly describe fogging and blurry or poor-quality images during use. There are 23 reports naming its identifier, with no deaths and 1 injury mentioned. No recalls name this device.

AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.

Adverse event reports
25
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 25 adverse event reports that list this exact device (DI 07613327062182), received between Apr 24, 2019 and Sep 1, 2026 — classified as 1 injury, 24 malfunctions.

The most frequently reported specific device problem is “Poor Quality Image” (13 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

Nov 2023: 1 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 1 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 1 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 2 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Poor Quality Image13
  • Fogging7
  • Optical Problem5
  • Adverse Event Without Identified Device or Use Problem1
  • Moisture Damage1
  • Moisture or Humidity Problem1
  • Nonstandard Device1
  • Optical Distortion1

Patient problems

  • No Clinical Signs, Symptoms or Conditions23
  • Insufficient Information5
  • Burn, Thermal1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 25 most recent of 25 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 1, 2026Poor Quality Image

    It was reported that it was blurry.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50554180 ↗
  • MalfunctionSep 1, 2026Fogging

    It was reported that the scope was cloudy with condensation inside the scope and the scope has been used since (b)(6) 2026, with only one sterilization cycle. The scope was replaced with another working scope at the start of the procedure. The moisture inside the scope cannot be wiped off because it was inside the scope lens.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 50534429 ↗
  • MalfunctionJun 19, 2026Fogging

    IT WAS REPORTED THAT THE ENDOSCOPE OFTEN FOGGED UP DURING USE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25564261 ↗
  • MalfunctionFeb 17, 2026Fogging

    IT WAS REPORTED THAT OPTICS GIVE FOGGY, UNCLEAR VISION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24372954 ↗
  • MalfunctionDec 11, 2025Fogging; Fogging

    THIS EVENT WAS INITIALLY REPORTED AS A MALFUNCTION FOR FOGGY IMAGE. UPON ADDITIONAL INFORMATION PROVIDED, THIS EVENT IS NO LONGER REPORTABLE. ADDTIONAL INFORMATION RECEIVED CONFIRMED THAT THERE WAS NO ASSOCIATED PROCEDURE ASSOCIATED WITH THIS COMPLAINT. THIS EVENT DESCRIPTION MOST LIKELY INDICATES ¿FOGGY IMAGE¿. THE REVIEW OF HISTORICAL COMPLAINT DATA, RISK DOCUMENTATION, AND THE REPORTED INFORMATION REGARDING THIS EVENT DO NOT SUGGEST A RECURRENCE OF THIS EVENT WOULD BE LIKELY TO RESULT IN A SERIOUS INJURY. NO ADVERSE CONSEQUENCES WERE DETERMINED TO BE REPORTABLE. THIS EVENT IS NO LONGER DETERMINED TO BE REPORTABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23782501 ↗
  • MalfunctionFeb 21, 2024Fogging; Optical Problem; Fogging; Optical Problem

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18753115 ↗
  • MalfunctionNov 17, 2023Fogging; Moisture or Humidity Problem; Fogging; Moisture or Humidity Problem

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18162069 ↗
  • MalfunctionAug 23, 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 17608209 ↗
  • MalfunctionAug 15, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17553150 ↗
  • MalfunctionAug 9, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17493924 ↗
  • MalfunctionAug 8, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17482538 ↗
  • MalfunctionAug 8, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17479895 ↗
  • MalfunctionAug 8, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17479894 ↗
  • MalfunctionAug 8, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17479892 ↗
  • MalfunctionAug 8, 2023Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17479891 ↗
  • MalfunctionApr 3, 2023Temperature Problem; Temperature Problem

    IT WAS REPORTED THAT THERE WAS A THERMAL EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16662823 ↗
  • MalfunctionOct 20, 2022Poor Quality Image; Poor Quality Image

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.

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

    MAUDE report 15638536 ↗
  • MalfunctionAug 31, 2022Optical Problem; Optical Problem

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15332283 ↗
  • MalfunctionAug 31, 2022Optical Problem; Optical Problem

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.

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

    MAUDE report 15330019 ↗
  • MalfunctionApr 18, 2022Optical Problem; Optical Problem

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14137326 ↗
  • MalfunctionFeb 17, 2022Fogging; Fogging

    IT WAS REPORTED THAT THERE WAS FOGGY IMAGE DURING PROCEDURE.

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

    MAUDE report 13552385 ↗
  • MalfunctionAug 31, 2021Poor Quality Image; Optical Distortion; Optical Distortion

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.

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

    MAUDE report 12393291 ↗
  • MalfunctionApr 7, 2021Poor Quality Image; Nonstandard Device; Poor Quality Image; Nonstandard Device

    IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.

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

    MAUDE report 11631593 ↗
  • MalfunctionMar 18, 2020Moisture Damage; Poor Quality Image; Moisture Damage

    IT WAS REPORTED THAT THE MOISTURE COULD NOT BE WIPED FROM THE SCOPE CAUSING AN UNCLEAR IMAGE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9850491 ↗
  • InjuryApr 24, 2019Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT WAS BURNED.

    Patient problems: Burn, Thermal

    MAUDE report 8545124 ↗

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Sources and updates

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