MAUDE Adverse Event Report: STERIS CORPORATION STERIS 5095 Surgical Table

Model Number	5095 Surgical Table
Medical Device Problem Code	Unintended Movement (3026)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/02/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
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.
Additional Manufacturer Narrative
The steris 5095 surgical table is being returned to for evaluation.Investigation in progress.A follow-up report will be submitted when additional information becomes available.

• Brand Name: STERIS 5095 Surgical Table
• Common Device Name: Surgical Table
• Manufacturer (Section D): STERIS CORPORATION; 2720 gunter park drive east; montgomery AL 36109
• Manufacturer (Section G): STERIS CORPORATION; 2720 gunter park drive east; montgomery AL 36109
• Manufacturer Contact: daniel davy ; 5960 heisley road; mentor, OH 44060 ; +1(440)259-7401
• MDR Report Key: 50098267
• Report Number: 1043572-2026-00077
• Device Sequence Number: 16031667
• Product Code: FQO
• UDI-Device Identifier: 00724995195649
• UDI-Public: (01)00724995195649(11)260402
• Combination Product (Y/N): N
• Initial Reporter Country: KS
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 07/31/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 5095 Surgical Table
• Device Catalogue Number: ST015211002
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/03/2026
• Initial Report FDA Received Date: 07/31/2026
• Date Device Manufactured: 04/02/2026
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown