Precision Ideal Eyes 0502904030Recalls & reported problems
Stryker Corporation · HD Arthroscope, Autoclavable, C-Mount, 30 ¿ 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 HD arthroscope is a sterilizable camera scope used to look inside joints during surgery. The 45 reports mostly describe image problems: blurry or poor quality pictures, lenses losing focus, and fogging inside the scope; a couple mention the device breaking during a procedure. There are 45 malfunction reports, with no deaths and no injuries. 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
- 49
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 49 adverse event reports that list this exact device (DI 07613327063844), received between May 13, 2019 and Sep 22, 2026 — classified as 49 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (32 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
- Poor Quality Image32
- Optical Problem16
- Fogging12
- Moisture or Humidity Problem3
- No Display/Image3
- Material Fragmentation2
- Nonstandard Device2
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions42
- Insufficient Information12
- No Known Impact Or Consequence To Patient8
Recent adverse event reports
The 25 most recent of 49 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 22, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50862556 ↗MalfunctionSep 9, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50702919 ↗MalfunctionSep 9, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50702915 ↗MalfunctionSep 9, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50697262 ↗MalfunctionAug 31, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50533111 ↗MalfunctionAug 7, 2026Poor Quality Image
It was reported that the lens loses focus, and creates a blurred image. Therefore, there was blurry image.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50182056 ↗MalfunctionAug 6, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50150618 ↗MalfunctionAug 5, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50150180 ↗MalfunctionMar 27, 2025Crack; Fogging; Crack; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21710118 ↗MalfunctionMar 27, 2025Fogging; 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 21709394 ↗MalfunctionNov 13, 2024Fogging; 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 20678579 ↗MalfunctionNov 8, 2024Break; Material Fragmentation; Break; Material Fragmentation
IT WAS REPORTED THAT THE DEVICE BROKE DURING PROCEDURE. THE BROKEN PIECE WAS SUCCESSFULLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20646030 ↗MalfunctionSep 4, 2024Fogging; 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 20134994 ↗MalfunctionNov 1, 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 18051588 ↗MalfunctionSep 20, 2023Fogging; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17785948 ↗MalfunctionSep 6, 2023Poor Quality Image; Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17695402 ↗MalfunctionApr 18, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16761978 ↗MalfunctionApr 7, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16704331 ↗MalfunctionApr 3, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16663424 ↗MalfunctionMar 30, 2023Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16650007 ↗MalfunctionJan 19, 2023Poor Quality Image
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16212191 ↗MalfunctionJan 19, 2023Fogging; Poor Quality Image; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16212188 ↗MalfunctionJan 19, 2023Fogging; Poor Quality Image; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16208674 ↗MalfunctionJan 19, 2023Fogging; Poor Quality Image; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16208671 ↗MalfunctionJan 19, 2023Fogging; Poor Quality Image; Fogging
IT WAS REPORTED THAT THERE WAS FOGGY IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16208127 ↗
Other ARTHROSCOPE devices
- FMS 283512Medos International Sàrl · ARTHROSCOPE1,800 reports
- Arthrex® AR-6480Arthrex, Inc. · ARTHROSCOPE949 reports
- FMS VUE 284002Depuy Mitek, LLC · ARTHROSCOPE829 reports
- MITEK 242018Medos International Sàrl · Arthroscope731 reports
- METRx® System 9560100Medtronic Sofamor Danek, Inc. · Arthroscope667 reports
- FMS VUE II 284004Medos International Sàrl · Arthroscope562 reports
- VAPR COOLPULSE 228146Depuy Mitek, LLC · ARTHROSCOPE474 reports
- FMS DUO 284580Depuy Mitek, LLC · ARTHROSCOPE458 reports
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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