Connected OR HubRecalls & reported problems across all models
Stryker Corporation · 2 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 137
- Deaths reported
- 1
- Injuries reported
- 2
- Recalls
- 0
We found 2 models of Connected OR Hub by Stryker Corporation in the FDA's device registry (GUDID). Together they are named in 137 adverse event reports in the FDA's MAUDE database, received between Jan 7, 2021 and Sep 30, 2026 — classified as 1 death, 2 injuries, 134 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (105 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 Connected OR Hub problems
Device problems
- No Display/Image105
- Output Problem28
- Connection Problem27
- Overheating of Device13
- Application Program Problem10
- Application Program Freezes or Fails to Launch9
- Erratic or Intermittent Display8
- Poor Quality Image8
Patient problems
- No Clinical Signs, Symptoms or Conditions114
- Insufficient Information35
- Bowel Perforation1
Connected OR Hub models
2 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Connected OR Hub 0240200100Arthroscope1 death124 reports
- Connected OR Hub 0240200200Laparoscope, general & plastic surgery13 reports
Recent Connected OR Hub adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Erratic or Intermittent Display; No Display/Image
Patient problems: Insufficient Information
MAUDE report 50953395 ↗MalfunctionSep 29, 2026Overheating of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50940524 ↗MalfunctionSep 23, 2026Erratic or Intermittent Display
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50863007 ↗MalfunctionSep 15, 2026Erratic or Intermittent Display
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50782086 ↗MalfunctionSep 14, 2026No Display/Image
It was reported that the images are flickering on the hub and wall monitors. Therefore there was flickering and there may have been a full loss of image.
Patient problems: Insufficient Information
MAUDE report 50760437 ↗MalfunctionSep 11, 2026Erratic or Intermittent Display; No Display/Image
Patient problems: Insufficient Information
MAUDE report 50744453 ↗MalfunctionSep 11, 2026Overheating of Device
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50744449 ↗InjurySep 9, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50699715 ↗MalfunctionSep 2, 2026No Display/Image
Patient problems: Insufficient Information
MAUDE report 50576358 ↗MalfunctionAug 31, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50529760 ↗MalfunctionAug 26, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50465025 ↗MalfunctionAug 26, 2026No Display/Image
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50463244 ↗MalfunctionAug 26, 2026Overheating of Device
It was reported that the device was overheating.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50444300 ↗MalfunctionJul 28, 2026No Display/Image
It was reported that the hub in an OR that is continuously shutting down mid case. The hub would shut down during almost every case however all cases were completed successfully. The estimated loss of image to be around 20 seconds per occurrence. Issues were noticed during procedure when the hub would shut down. The same device was used to complete all cases. No medical intervention was needed. No adverse consequences as visualization come back quickly and media was saved. The estimated delay to be about 5 minutes per case if the hub only shut down once. No patient impact was reported. The HUB was reported to have the same event occur 10 times.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50060427 ↗MalfunctionJun 12, 2026No Display/Image
IT WAS REPORTED THAT IN THE MIDDLE OF THE PROCEDURE THE CONNECTED OR HUB SHUT DOWN AND THEN HAD TO RESTART IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25484952 ↗
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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