Ideal Eyes, Speed-Lock 0502204030Recalls & reported problems
Stryker Corporation · Long 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
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327053623), received between Nov 14, 2018 and May 6, 2026 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (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
- Poor Quality Image3
- Material Fragmentation2
- Material Integrity Problem2
- Nonstandard Device1
- Optical Problem1
- Unintended Collision1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
- Insufficient Information2
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 6, 2026Material Fragmentation; Material Integrity Problem
IT WAS REPORTED THAT 30 DEGREE SCOPE SNAPPED DURING HIP SCOPE PROCEDURE. THEY USED A REPLACEMENT SCOPE FOR THE REMAINDER OF THE PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25105284 ↗MalfunctionOct 9, 2023Poor Quality Image; Material Integrity Problem; Poor Quality Image; Material Integrity Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17896430 ↗MalfunctionJun 2, 2021Nonstandard Device; Poor Quality Image; Nonstandard Device
IT WAS REPORTED THAT THERE WAS UNCLEAR IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11925773 ↗MalfunctionMay 6, 2021Poor Quality Image; Optical Problem; Optical Problem
IT WAS REPORTED THAT THERE WAS BLURRY IMAGE DURING PROCEDURE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11787932 ↗InjuryNov 14, 2018Material Fragmentation; Unintended Collision
IT WAS REPORTED THE SCOPE LOOKS LIKE IT SUSTAINED DAMAGE FROM A BURR HITTING THE TIP RESULTING IN PIECES BREAKING INSIDE THE PATIENT. CANNOT CONFIRM IF THE PIECES BROKE OFF WERE RETRIEVED.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 8069712 ↗
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- 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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