Connected OR Cart 240099155Recalls & reported problems
Stryker Corporation · . · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
Quick summary
This Stryker Connected OR Cart is equipment used in operating rooms. There are 24 adverse event reports naming its identifier, with no deaths and no injuries; all describe malfunctions, most often the screen or image going out during a procedure, the cart losing power, or the arm drifting, and one report mentions the device smoking. No recalls name this device. Reports have slowed, with 1 in the past 12 months compared with 7 in the prior 12 months.
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
- 24
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 24 adverse event reports that list this exact device (DI 00858701006360), received between Feb 24, 2020 and Dec 18, 2025 — classified as 24 malfunctions.
The most frequently reported specific device problem is “No Display/Image” (13 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- No Display/Image13
- Mechanical Problem6
- Electrical Power Problem2
- Electrical Shorting2
- Loss of Power2
- Output Problem2
- Positioning Problem2
- Arcing1
Patient problems
- No Clinical Signs, Symptoms or Conditions23
- Insufficient Information3
- No Consequences Or Impact To Patient1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 24 most recent of 24 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 18, 2025No Display/Image; Electrical Shorting; No Display/Image; Electrical Shorting
IT WAS REPORTED THAT THE CART SHUT OFF MID CASE. NO PATIENT HARM OR SURGICAL DELAY. THEREFORE, THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23843440 ↗MalfunctionMay 7, 2025No Display/Image; Electrical Shorting; No Display/Image; Electrical Shorting
IT WAS REPORTED THAT THE CONNECTED OR CART ABRUPTLY LOST POWER DURING PROCEDURE. THEREFORE, THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21981419 ↗MalfunctionApr 15, 2025No Display/Image; Electrical Power Problem; No Display/Image; Electrical Power Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21838678 ↗MalfunctionApr 11, 2025No Display/Image; Electrical Power Problem; No Display/Image; Electrical Power Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21827859 ↗MalfunctionFeb 27, 2025No Display/Image; Connection Problem; No Display/Image; Connection Problem
IT WAS REPORTED THAT THERE LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21484607 ↗MalfunctionFeb 27, 2025Smoking; Temperature Problem; Smoking; Temperature Problem
IT WAS REPORTED THAT THERE WAS THERMAL EVENT DUE TO THE DEVICE SMOKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21483324 ↗MalfunctionFeb 10, 2025No Display/Image; Product Quality Problem; No Display/Image; Product Quality Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21348338 ↗MalfunctionDec 11, 2024Positioning Problem; Positioning Problem
IT WAS REPORTED THAT THE CART ARM WAS DRIFTING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20907792 ↗MalfunctionDec 6, 2023No Display/Image; No Display/Image
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18279530 ↗MalfunctionNov 15, 2023No Display/Image; No Device Output; No Display/Image; No Device Output
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18145559 ↗MalfunctionOct 25, 2023No Display/Image; Output Problem; No Display/Image; Output Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18007739 ↗MalfunctionAug 7, 2023No Display/Image; No Display/Image
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17476575 ↗MalfunctionJul 31, 2023No Display/Image; Output Problem; No Display/Image; Output Problem
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17430845 ↗MalfunctionJul 26, 2023Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT THERE WAS DRIFTING OF THE CART ARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17401520 ↗MalfunctionJul 24, 2023Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT THERE WAS DRIFTING OF THE CART ARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17385133 ↗MalfunctionJul 20, 2023Mechanical Problem; Mechanical Problem
IT WAS REPORTED THAT THERE WAS DRIFTING OF THE CART ARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17367800 ↗MalfunctionJun 29, 2023Mechanical Problem; Mechanical Problem
IT WAS REPORTED THE CART ARM WAS DRIFTING. THERE WAS NO REPORT OF PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17231970 ↗MalfunctionOct 20, 2022Mechanical Problem; Positioning Problem; Mechanical Problem
IT WAS REPORTED THE CART ARM WAS DRIFTING. THERE WAS NO REPORT OF PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15638535 ↗MalfunctionJul 25, 2022Display or Visual Feedback Problem; Material Integrity Problem; Material Integrity Problem
IT WAS REPORTED THAT THE DEVICE LOST IMAGE DURING A CASE. THERE WAS A 15 MINUTE DELAY WHILE REPLACING THE DEVICE. THERE IS NO REPORT OF ADVERSE CONSEQUENCES AS A RESULT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15095250 ↗MalfunctionMay 25, 2022Mechanical Problem; Unintended Movement; Mechanical Problem
IT WAS REPORTED THE CART ARM WAS DRIFTING. THERE WAS NO REPORT OF PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14496617 ↗MalfunctionJan 12, 2022Arcing
IT WAS REPORTED THAT THERE WAS ARCING BETWEEN THE CABLES.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 13237824 ↗MalfunctionMay 10, 2021No Display/Image; Unintended System Motion; Unintended System Motion
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11803359 ↗MalfunctionFeb 17, 2021Loss of Power; No Display/Image; Loss of Power
IT WAS REPORTED THAT THERE WAS LOSS OF IMAGE.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11338486 ↗MalfunctionFeb 24, 2020Loss of Power; Intermittent Loss of Power; Intermittent Loss of Power
IT WAS REPORTED THAT THERE WAS LOSS OF VISUALIZATION DURING PROCEDURE, CAUSED BY INTERMITTENT POWER LOSS OF THE CONNECTED OR CART. PLEASE NOTE THAT THE PROCEDURE WAS COMPLETED SUCCESSFULLY, WITH NO REPORTS OF ADVERSE CONSEQUENCES.
Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient
MAUDE report 9746076 ↗
Other CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT) devices
- Drive 13002SV-1Drive Devilbiss Healthcare · CART, EMERGENCY, CARDIOPULMONARY (EXCLUDING EQUIPMENT)1 report
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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