Ideal Eyes, Speed-Lock 0502104030Recalls & reported problems
Stryker Corporation · Arthroscope, Autoclavable, 30 ¿ View Direction · Class 2
All models of Ideal Eyes, Speed-Lock (7)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Stryker Ideal Eyes arthroscope is an autoclavable arthroscope. Reports mostly describe blurry or foggy images during use, sometimes leading to use of another scope. There are 81 adverse event reports, no deaths and 2 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
- 100
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 100 adverse event reports that list this exact device (DI 07613327062113), received between Jun 27, 2019 and Sep 30, 2026 — classified as 2 injuries, 98 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (51 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 Image51
- Optical Problem46
- Fogging27
- No Display/Image3
- Break1
- Crack1
- Display or Visual Feedback Problem1
- Material Integrity Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions87
- Insufficient Information22
- No Known Impact Or Consequence To Patient8
- Device Embedded In Tissue or Plaque1
- Injury1
Recent adverse event reports
The 25 most recent of 100 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953983 ↗MalfunctionSep 30, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50953981 ↗MalfunctionSep 29, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940819 ↗MalfunctionSep 29, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50933277 ↗MalfunctionSep 23, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876307 ↗MalfunctionSep 23, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876265 ↗MalfunctionSep 23, 2026Poor Quality Image
It was reported that the scope had blurry image and the lens might be damaged.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872779 ↗MalfunctionSep 23, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872568 ↗MalfunctionSep 23, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50872561 ↗MalfunctionSep 18, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50830956 ↗MalfunctionSep 17, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50810829 ↗MalfunctionSep 16, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794041 ↗MalfunctionSep 14, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765048 ↗MalfunctionSep 14, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765046 ↗MalfunctionSep 14, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50763650 ↗MalfunctionSep 11, 2026Poor Quality Image
It was reported that the scope did not produce a clear image.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50725369 ↗MalfunctionSep 9, 2026Poor Quality Image
It was reported that the scope was blurry.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50681591 ↗MalfunctionSep 2, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50576496 ↗MalfunctionSep 1, 2026Poor Quality Image
It was reported that the scope was blurry and the original scope was not used for completing the procedure.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50534430 ↗MalfunctionAug 31, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50533824 ↗MalfunctionAug 27, 2026Poor Quality Image
It was reported that the scope was blurry.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50487892 ↗MalfunctionAug 11, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50202657 ↗MalfunctionAug 7, 2026Poor Quality Image
It was reported that there was blurry image.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50182211 ↗MalfunctionJul 28, 2026
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50058152 ↗MalfunctionJul 28, 2026
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50058150 ↗
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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