Ideal Eyes, Speed-LockRecalls & reported problems across all models
Stryker Corporation · 7 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 133
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls
- 0
We found 7 models of Ideal Eyes, Speed-Lock by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 133 adverse event reports in the FDA's MAUDE database, received between Nov 14, 2018 and Sep 30, 2026 — classified as 5 injuries, 128 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (74 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. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Ideal Eyes, Speed-Lock problems
Device problems
- Poor Quality Image74
- Optical Problem55
- Fogging31
- Material Integrity Problem4
- No Display/Image4
- Break3
- Nonstandard Device3
- Material Fragmentation2
Patient problems
- No Clinical Signs, Symptoms or Conditions117
- Insufficient Information32
- No Known Impact Or Consequence To Patient12
- Device Embedded In Tissue or Plaque2
- Injury1
Ideal Eyes, Speed-Lock models
7 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Ideal Eyes, Speed-Lock 0502104030ARTHROSCOPE100 reports
- Ideal Eyes, Speed-Lock 0502204070ARTHROSCOPE12 reports
- Ideal Eyes, Speed-Lock 0502704030ARTHROSCOPE8 reports
- Ideal Eyes, Speed-Lock 0502204030ARTHROSCOPE5 reports
- Ideal Eyes, Speed-Lock 0502127030ARTHROSCOPE3 reports
- Ideal Eyes, Speed-Lock 0502104010ARTHROSCOPE3 reports
- Ideal Eyes, Speed-Lock 0502104070ARTHROSCOPE2 reports
Recent Ideal Eyes, Speed-Lock adverse event reports
The 15 most recent reports across all models, 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 25, 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 50897984 ↗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 ↗
Other Stryker Corporation products
- RemB7 models · 3,073 reports
- Prime Series21 models · 1,548 reports · 2 recalls
- TARGET114 models · 1,077 reports
- ProCuity17 models · 368 reports · 13 recalls
- Spetzler-Malis20 models · 7 reports · 19 recalls
- SYNCHRO 28 models · 313 reports · 9 recalls
- Neptune E-SEP19 models · 412 reports · 7 recalls
- StrykeFlow4 models · 552 reports · 4 recalls
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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