STERIS 4095 Surgical TableRecalls & reported problems
Steris Corporation · STERIS 4095 TABLE 120V SS VELCRO 2-inch TLT PADS · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00724995195281), received between Apr 2, 2024 and Jul 17, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Tipped Over” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device Tipped Over1
- Mechanical Problem1
- Positioning Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 17, 2025Mechanical Problem; Mechanical Problem
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 4095 SURGICAL TABLE WOULD NOT LOWER IN HEIGHT WHEN COMMANDED. USER FACILITY PERSONNEL ELECTED TO CONTINUE THE PROCEDURE WHICH WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22529493 ↗MalfunctionNov 15, 2024Positioning Problem; Positioning Problem
THE USER FACILITY REPORTED THAT THE HEAD AND TORSO SECTION TO THEIR 4095 SURGICAL TABLE "MOVED DOWN" DURING A PATIENT PROCEDURE. THE PATIENT WAS TRANSFERRED TO ANOTHER SURGICAL TABLE RESULTING IN A PROCEDURE DELAY. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20694327 ↗MalfunctionApr 2, 2024Device Tipped Over; Device Tipped Over
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 4095 SURGICAL TABLE WAS FOUND TIPPED TOWARDS THE HEAD END AND THE FOOT END OF THE TABLE HAD LIFTED OFF THE FLOOR. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19020966 ↗
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- 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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.