STERIS 5085 SRT Surgical Table (REF ST014807)Recalls & reported problems
Steris Corporation · The STERIS 5085 SRT Surgical Table Battery Line with Featherweight Leg Section and TLT Pads has an innovative 5th wheel design allows one caregiver to safely and easily move patients from pre-op to OR to post-op. · 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 00724995154998), received between May 6, 2026 and May 6, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Key or Button Unresponsive/not Working” (1 report).
4 other recalls cover devices cleared under the same FDA submission (K090136); they may or may not involve this specific model.
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
- Key or Button Unresponsive/not Working1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 6, 2026Key or Button Unresponsive/not Working
THE USER FACILITY REPORTED THAT WHILE TRANSFERRING A PATIENT TO THEIR 5085 SRT SURGICAL TABLE, THE PATIENT'S LEG BEGAN TO SLIP; HOWEVER, THE USER FACILITY PERSONNEL REPOSITIONED THEIR LEG ON THE TABLE. ADDITIONALLY, USER FACILITY REPORTED THAT THE HAND CONTROL WAS NOT RESPONDING TO COMMANDS. USER FACILITY PERSONNEL ELECTED TO PROCEED WITH THE PROCEDURE WHICH WAS COMPLETED SUCCESSFULLY ON THE SAME TABLE. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25095572 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K090136. One submission often covers many models, so check the product and lot details in each record.
- Z-0196-2015 · Oct 10, 2014 · TerminatedThe 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal table top elevation.
- Z-2426-2012 · Apr 6, 2012 · TerminatedSTERIS 5085 and 5085 SRT Surgical Tables, Product Usage: The 5085 is a general surgical table with high patient weight capacity, extended width capability, and lower minimal tab
- Z-0279-2012 · Oct 17, 2011 · TerminatedSTERIS 5085 and 5085SRT Surgical Tables, Catalog Numbers: 5085- ST01-410-1; 5085SRT- ST0-1420-6.
- Z-1941-2010 · May 14, 2010 · TerminatedSTERIS 4085, 5085 & 5085SRT Surgical Tables
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.
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