Precision IE 4KRecalls & reported problems across all models
Stryker Corporation · 11 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 212
- Deaths reported
- 0
- Injuries reported
- 10
- Recalls
- 0
We found 11 models of Precision IE 4K by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 212 adverse event reports in the FDA's MAUDE database, received between Jul 29, 2019 and Sep 30, 2026 — classified as 10 injuries, 202 malfunctions.
The most frequently reported specific device problem is “Poor Quality Image” (116 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 Precision IE 4K problems
Device problems
- Poor Quality Image116
- Fogging71
- Optical Problem55
- Crack10
- Adverse Event Without Identified Device or Use Problem7
- Moisture or Humidity Problem4
- Optical Distortion3
- Insufficient Device Problem Information2
Patient problems
- No Clinical Signs, Symptoms or Conditions196
- Insufficient Information20
- No Known Impact Or Consequence To Patient14
- Unspecified Tissue Injury5
Precision IE 4K models
11 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Precision IE 4K 0502-444-030Arthroscope91 reports
- Precision IE 4K 0502-404-030Arthroscope75 reports
- Precision IE 4K 0502-445-030Arthroscope10 reports
- Precision IE 4K 0502-444-070Arthroscope9 reports
- Precision IE 4K 0502-445-070Arthroscope6 reports
- Precision IE 4K 0502-404-070Arthroscope6 reports
- Precision IE 4K 0502-414-030Arthroscope6 reports
- Precision IE 4K 0502-414-070Arthroscope5 reports
- Precision IE 4K 0502-276-030Arthroscope2 reports
- Precision IE 4K 0502-444-010Arthroscope1 report
- Precision IE 4K 0502-404-010Arthroscope1 report
Recent Precision IE 4K 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; Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50954459 ↗MalfunctionSep 29, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940509 ↗MalfunctionSep 24, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50886490 ↗MalfunctionSep 23, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876306 ↗MalfunctionSep 23, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50876274 ↗MalfunctionSep 21, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50848341 ↗MalfunctionSep 18, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50831063 ↗MalfunctionSep 16, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794456 ↗MalfunctionSep 16, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794452 ↗MalfunctionSep 16, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794238 ↗MalfunctionSep 16, 2026Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50794039 ↗MalfunctionSep 14, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765826 ↗MalfunctionSep 14, 2026Fogging; Poor Quality Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50765760 ↗MalfunctionSep 11, 2026Fogging
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744512 ↗MalfunctionSep 11, 2026Fogging
It was reported that the scope had foggy lens and the fogginess was not able to be wiped off when attempted to wipe.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50735027 ↗
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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