EZ Slide 3503Recalls & reported problems
Skytron LLC · EZ-SLIDE · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10841736112165), received between Jun 16, 2023 and Jun 16, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Electrical /Electronic Property Problem” (1 report).
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.
Most reported problems
Device problems
- Electrical /Electronic Property Problem1
- Lack of Effect1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Burn(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 16, 2023Electrical /Electronic Property Problem; Lack of Effect; Electrical /Electronic Property Problem; Lack of Effect
HERE WAS A FIRE IN THEIR OPERATING ROOM AFTER THEY HEARD POPPING AND SPARKING SOUNDS COMING FROM THE POWER OUTLET ON THE OPERATING TABLE IN THE HOSPITAL. THE HOSPITAL SUSPECTS THAT THE CAUSE COULD HAVE BEEN LIQUID GETTING INTO THE OUTLET. THE FAILURE OCCURRED OUTSIDE OF THE SURGERY. THE DISTRIBUTOR CONFIRMED THAT THE CUSTOMER HAD USED A BEACH CHAIR TO ATTACH TO THE OPERATING TABLE. THE BEACH CHAIR WAS WET AT THE TIME, WHICH MAY HAVE ALLOWED LIQUID TO ENTER THE ELECTRICAL CONNECTORS OF THE OPERATING TABLE. IN ADDITION, THE FACILITY USED AN UNAUTHORIZED POWER CORD. THE MANUFACTURER DISCUSSED POSSIBLE CAUSES FOR THE INCIDENT. THE MOST LIKELY SCENARIO IS THAT THE ENTRY OF LIQUID, DUST, AND OTHER CONTAMINANTS INTO THE ELECTRICAL CONNECTORS OF THE OPERATING TABLE CAUSED A SHORT CIRCUIT. THIS, IN TURN, RESULTED IN EXCESSIVE CURRENT FLOW LEADING TO IGNITION. THE USE OF AN UNAUTHORIZED POWER CORD COULD ALSO HAVE CAUSED THE SHORT CIRCUIT. HOWEVER, THE EXACT CAUSE OF THE INCIDENT REMAINS UNDETERMINED AS WE HAVE NOT BEEN ABLE TO EXAMINE THE ACTUAL PRODUCT. THE OWNER'S MANUAL STATES THAT CAUTION SHOULD BE TAKEN WHEN CLEANING THE TABLE TO PREVENT EXCESSIVE FLUID ENTRY INTO ELECTRICAL CONNECTORS,
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Burn(s)
MAUDE report 17148961 ↗
Other Table, Operating-Room, Ac-Powered devices
- ORT300 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls21 reports
- ORT200 TableIMRIS Imaging, Inc. · Table, Operating-Room, Ac-Powered2 recalls12 reports
- MEERA mobile operating table 720001F2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page