Connected OR Hub 0240200100Recalls & reported problems
Stryker Corporation · Device Management Control System · Class 2
All models of Connected OR Hub (2)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Quick summary
This Stryker Connected OR hub is an operating room device management system. Reports describe the hub losing its image or shutting down mid-case, overheating warnings, connection problems and software that freezes or fails to launch. There are 114 reports, including 1 death and 1 injury. 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
- 124
- Deaths reported
- 1
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 124 adverse event reports that list this exact device (DI 07613327413281), received between Jan 7, 2021 and Sep 30, 2026 — classified as 1 death, 2 injuries, 121 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (93 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
- No Display/Image93
- Output Problem25
- Connection Problem23
- Overheating of Device12
- Application Program Problem10
- Application Program Freezes or Fails to Launch8
- Poor Quality Image8
- Erratic or Intermittent Display6
Patient problems
- No Clinical Signs, Symptoms or Conditions104
- Insufficient Information31
- Bowel Perforation1
Recent adverse event reports
The 25 most recent of 124 reports, 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 ↗MalfunctionMay 14, 2026No Display/Image; Overheating of Device
IT WAS REPORTED THAT HUB CONNECTED TO A CORLITE SYSTEM ALERTED THAT IT WAS OVERHEATING AND WOULD SHUT DOWN DUE TO HEAT. THE ACCOUNT THEN HAD 45 SECONDS BEFORE THE HUB POWERED DOWN. THIS HUB IS NOT IN AN ENCLOSED SPACE AND TO BE HONEST ITS PROBABLY GIVEN SOME OF THE BEST CLEARANCE FROM OTHER OBJECTS IN AN OR SPACE THAT HE HAVE SEEN. HUB WAS OFF WHEN HE VISITED AND WAS NOT HOT TO TOUCH. IMAGE LOSS DUE TO CORLITE SETUP NO LONGER BEING ABLE TO ROUTE THROUGH HUB DURING CASE. BACKUP SIGNAL UTILIZED AND THAT WORKED FINE. UNSURE OF DURATION OF LOSS OF IMAGE. LIKELY UNTIL THEY WAS ABLE TO REMIND THEM OF THEIR BACKUP SIGNAL ON MONITOR 1 IN THE ROOM. PROCEDURE WAS COMPLETED USING BACKUP SIGNAL DIRECTLY TO MONITOR 1 FROM ENDOCAMERA CONTROL UNIT. THEREFORE, THERE WAS A THERMAL EVENT AND LOSS OF IMAGE.
Patient problems: Insufficient Information
MAUDE report 25172991 ↗MalfunctionApr 24, 2026No Display/Image; Output Problem
IT WAS REPORTED THAT IN OR2 HUB SHUT DOWN IN THE MIDDLE OF A CASE AND BOTTOM BATTERY IN RACK WAS ORANGE. THEREFORE, THERE WAS A LOSS OF IMAGE.
Patient problems: Insufficient Information
MAUDE report 24987772 ↗MalfunctionMar 26, 2026Computer Software Problem; No Display/Image
IT WAS REPORTED THAT THERE WAS SOFTWARE ISSUE. THE COR II HUB 3.2.2 RECENTLY STARTED INTERMITTENTLY RESTARTING 2 (AFFECTED) OUT OF 5 ROOMS. ISSUED RECOMMENDATION TO UPDATE TO 4.1.2 & TURN OFF WIFI SYSTEM USING ETHERNET AND WIFI OFF WHEN THE ETHERNET CORD WAS UNPLUGGED, THE ISSUE WENT AWAY. OBVIOUSLY WHEN THE HUB WAS TURNING OFF AND ON, THERE WAS A LOSS OF IMAGE. THERE WAS NO PATIENT INVOLVEMENT/IMPACT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24700091 ↗MalfunctionMar 18, 2026Overheating of Device
IT WAS REPORTED THAT THERE WAS A SMELL OF BURNING PLASTIC. NO MEDICAL DELAY BUT HAPPENED DURING CASE. SN (B)(6).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24632717 ↗MalfunctionFeb 25, 2026No Display/Image; Connection Problem
IT WAS REPORTED THAT THE HUB POWER CYCLED DURING A PROCEDURE AND THE MEDIA WAS LOST. THIS COULD BE A HUB OR MNA ISSUE. REQUIRES TECH TO INVESTIGATE.
Patient problems: Insufficient Information
MAUDE report 24448761 ↗MalfunctionFeb 18, 2026No Display/Image; Output Problem
IT WAS REPORTED THAT THE INTEGRATION SYSTEM SHUT OFF DURING A CASE. THE SYSTEM EVENTUALLY REBOOTED AND WAS ABLE TO RESUME USE. NO INFORMATION ABOUT DURATION OF LOSS OF IMAGE IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24383913 ↗MalfunctionFeb 18, 2026No Display/Image; Output Problem
IT WAS REPORTED THAT THE INTEGRATION SYSTEM SHUT OFF DURING A CASE. THE SYSTEM EVENTUALLY REBOOTED AND WAS ABLE TO RESUME USE. NO INFORMATION ABOUT DURATION OF LOSS OF IMAGE IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24383684 ↗MalfunctionFeb 18, 2026No Display/Image; Application Program Problem
IT WAS REPORTED THAT THE DEVICE SHUT DOWN IN MIDDLE OF CASE, OS SLOW/LAG WHEN RETEST FULL LOSS OF IMAGE REPORTED BY NURSE. DURATION OF LOSS OF IMAGE WAS UNKNOWN. STAFF BROUGHT IN NEW TOWER FOR PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24381791 ↗MalfunctionFeb 12, 2026No Display/Image
IT WAS REPORTED THAT OOBF HUB KEEPS HAVING ISSUES AFTER PREVIOUS REPAIR, ALL SOURCES STOP WORKING, WINDOW POPS UP SOME SYSTEM SERVICES HAVE STOPPED WORKING PLEASE REBOOT AND CONTACT STRYKER TECH SUPPORT. SLIGHT DELAY 5 MINUTES. ALL THE SOURCES RANDOMLY FELL OFF THE HUB. THEY WOULD CONTINUALLY GET THE SPINNING WHEEL AND WOULD HAVE TO REBOOT. ONCE THEY GO TO SOURCES TO ROUTE NOTHING IS THERE. WHEN THEY HIT NEW CASE GET THE WHEEL AGAIN. PROCEDURE COMPLETED USING A VIDEO TOWER. HENCE THERE WAS A LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24322300 ↗MalfunctionFeb 4, 2026No Display/Image; Output Problem
IT WAS REPORTED THAT THEY HAD ORS WITH HUB THAT ARE RANDOMLY POWERING OFF AND ON- ALL MONITORS LOST SIGNAL.
Patient problems: Insufficient Information
MAUDE report 24261467 ↗
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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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