STERIS 5095 Surigical Table (REF ST015211002)Recalls & reported problems
Steris Corporation · The STERIS 5095 General Surgical Table, SS Featherweight Leg Section Velcro 2-inch TLT Pads is a flexible design gives OR staff the versatility they need to perform a wide range of surgeries using a variety of patient positions. · Class 1
- Adverse event reports
- 17
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 17 adverse event reports that list this exact device (DI 00724995195649), received between Jun 2, 2022 and Jul 31, 2026 — classified as 1 injury, 16 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (6 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement6
- Adverse Event Without Identified Device or Use Problem2
- Leak/Splash2
- Detachment of Device or Device Component1
- Device Handling Problem1
- Failure to Align1
- Improper or Incorrect Procedure or Method1
- Insufficient Device Problem Information1
Patient problems
- No Clinical Signs, Symptoms or Conditions12
- Abrasion2
- Discomfort2
- Pain1
Recent adverse event reports
The 17 most recent of 17 reports, in the reporter's own words as published by the FDA.
InjuryJul 31, 2026Unintended Movement
The user facility reported during a patient procedure while their STERIS 5095 Surgical Table was in Reverse Trendelenburg position that the seat section began to move "downward" without being commanded to do so. User facility personnel utilized the hand control to raise the seat section, and the procedure was completed successfully without delay. No report of injury.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50098267 ↗MalfunctionJul 9, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Abrasion
MAUDE report 25771030 ↗MalfunctionApr 17, 2026Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THEIR 5095 SURGICAL TABLE BEGAN TO TIP AND A PATIENT BEGAN TO SLIDE WHILE THE TABLE WAS BEING PUT IN TRENDELENBURG POSITION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY AND THE PATIENT DID NOT FALL OFF THE TABLE. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24914496 ↗MalfunctionFeb 19, 2026Leak/Splash
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR 5095 SURGICAL TABLE WOULD NOT HOLD THE COMMANDED POSITION. USER FACILITY PERSONNEL STATED THAT FLUID WAS ALSO LEAKING FROM THE BASE OF THE TABLE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY AND NO INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24390979 ↗MalfunctionDec 22, 2025Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR 5095 SURGICAL TABLE WAS IN REVERSE TRENDELENBURG POSITION, WHEN THE FOOT END OF THE TABLE "ABRUPTLY DROPPED DOWN" CAUSING THE HEAD SECTION TO RISE UPWARDS. USER FACILITY PERSONNEL STATED A "LOUD NOISE" WAS HEARD DURING THE MOVEMENT. USER FACILITY PERSONNEL ELECTED TO CANCEL THE PROCEDURE.
Patient problems: Pain
MAUDE report 23863112 ↗MalfunctionDec 11, 2025Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED THAT WHILE TRANSFERRING A PATIENT TO A BED, THEIR 5095 SURGICAL TABLE BEGAN TO SLIDE. NO REPORT OF INJURY OR PROCEDURE DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23783892 ↗MalfunctionJul 16, 2025Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE A PATIENT SLID TOWARDS THE HEAD SECTION TO THEIR 5095 SURGICAL TABLE WHILE THE TABLE WAS IN THE TRENDELENBURG POSITION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22525024 ↗MalfunctionMay 21, 2025Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method
THE USER FACILITY REPORTED THAT WHILE A PATIENT WAS POSITIONED ON THEIR 5095 SURGICAL TABLE, THE DUAL ARTICULATING HEADREST "COLLAPSED" SUBSEQUENTLY CAUSING THE PATIENT TO SUSTAIN AN INJURY. USER FACILITY PERSONNEL ELECTED TO CANCEL THE PROCEDURE.
Patient problems: Abrasion
MAUDE report 22062143 ↗MalfunctionApr 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE USER FACILITY REPORTED THAT THE FLOOR LOCKS TO THEIR 5095 SURGICAL TABLE WERE NOT OPERATING PROPERLY. THE PATIENT WAS TRANSFERRED TO A DIFFERENT SURGICAL TABLE AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY FOLLOWING A SHORT DELAY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21778670 ↗MalfunctionFeb 7, 2025Failure to Align; Failure to Align
THE USER FACILITY REPORTED THE FLOOR LOCKS TO THEIR 5095 SURGICAL TABLE WOULD NOT ENGAGE PROPERLY. USER FACILITY PERSONNEL HAD TO MANUALLY LOCK THE TABLE, RESULTING IN A SHORT DELAY IN A PATIENT PROCEDURE. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21336784 ↗MalfunctionJan 8, 2025Unintended Movement; Unintended Movement
THE USER FACILITY REPORTED DURING A PATIENT PROCEDURE THAT THEIR 5095 SURGICAL TABLE SLID DOWN WITHOUT BEING COMMANDED TO DO SO. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21103928 ↗MalfunctionJul 25, 2024Leak/Splash; Leak/Splash
THE USER FACILITY REPORTED THAT AT THE CONCLUSION OF A PATIENT PROCEDURE IT WAS OBSERVED THAT HYDRAULIC FLUID WAS LEAKING FROM THEIR 5095 SURGICAL TABLE. THE PATIENT PROCEDURE WAS COMPLETED SUCCESSFULLY HOWEVER, THE FOLLOWING PROCEDURE WAS DELAYED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19829375 ↗MalfunctionMay 23, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE THE DOCTOR RAISED THE LEG SECTION OF THEIR 5095 SURGICAL TABLE CAUSING THE E-Z LIFT BEACH CHAIR TO FALL OFF THE TABLE AND ONTO THE FLOOR. THE PATIENT WAS NOT INJURED. A PROCEDURE DELAY OCCURRED AS THE PATIENT WAS REPOSITIONED AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19386168 ↗MalfunctionFeb 23, 2024Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT PRIOR TO THE START OF A PATIENT PROCEDURE THE FLOOR LOCKS ON (B)(4) OF THEIR (B)(4) SURGICAL TABLES WOULD NOT DISENGAGE FROM THE FLOOR AND IN ADDITION (B)(4) OF THE TABLES WAS LEAKING OIL NEAR THE LEG OF THE TABLE. A 15-MINUTE DELAY OCCURRED AS A RESULT OF THE EVENT. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18768382 ↗MalfunctionSep 18, 2023Mechanical Problem; Insufficient Device Problem Information; Mechanical Problem; Insufficient Device Problem Information
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, THEIR 5095 SURGICAL TABLE "STOPPED WORKING". NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17769492 ↗MalfunctionAug 18, 2022Device Handling Problem; Device Handling Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE HAD GRABBED A HEADREST FOR THE 5095 SURGICAL TABLE FROM THEIR STORAGE AREA AND WHILE TRANSPORTING THE HEADREST THE EMPLOYEE'S FINGERS WERE PINCHED. THE EMPLOYEE RECEIVED X-RAYS AND ICE WAS APPLIED.
Patient problems: Discomfort
MAUDE report 15254624 ↗MalfunctionJun 2, 2022Physical Resistance/Sticking; Physical Resistance/Sticking
THE USER FACILITY REPORTED THAT DURING A PATIENT PROCEDURE, AN EMPLOYEE OBTAINED AN INJURY TO THEIR BACK WHILE ATTEMPTING TO RE-POSITION ONE OF THEIR 5095 SURGICAL TABLES THAT WAS STICKING TO THE FLOOR. NO REPORT OF PROCEDURE DELAY. THE USER FACILITY DID NOT DISCLOSE IF MEDICAL TREATMENT WAS SOUGHT OR ADMINISTERED.
Patient problems: Discomfort
MAUDE report 14573588 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.