MAUDE Adverse Event Report: STERIS CORPORATION; SURGICAL TABLE

Model Number	7080 SURGICAL TABLE
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/05/2026
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event and observed that the table was displaying two fault codes indicating the actuators required calibration.The technician further observed that the column shrouds were misaligned.The technician calibrated the actuators, realigned the column shrouds, tested the function and operation of the surgical table, confirmed it to be operating to specification and returned the table to service.No additional issues have been reported.
Event or Problem Description
The user facility reported that while a patient was being transferred onto their 7080 surgical table for a procedure, the table would not respond to commands.User facility personnel utilized another surgical table, and the procedure was completed successfully following a short delay.No report of injury.

• Brand Name: NA
• 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 ; 4402597401
• MDR Report Key: 25399703
• Report Number: 1043572-2026-00054
• Device Sequence Number: 16131974
• Product Code: FQO
• UDI-Device Identifier: 00724995229139
• UDI-Public: (01)00724995229139(11)250530
• Combination Product (Y/N): N
• Initial Reporter State: CA
• Initial Reporter Country: US
• 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): 06/04/2026

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: 7080 SURGICAL TABLE
• Device Catalogue Number: ST017311002
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/05/2026
• Initial Report FDA Received Date: 06/04/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/30/2025
• 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