MAUDE Adverse Event Report: STERIS CORPORATION; SURGICAL TABLE

Model Number	7080 SURGICAL TABLE
Medical Device Problem Code	Use of Device Problem (1670)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/04/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that during a patient procedure, user facility personnel commanded their 7080 surgical table into reverse trendelenburg and the table's foot section "dropped quickly" to the floor as well as the head section.The patient was transferred to another table where the procedure was completed successfully following a short delay.No report of injury.
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event to inspect the 7080 surgical table.During follow-up with user facility personnel, he was informed that when the table was commanded into reverse trendelenburg, the leg section became obstructed by a stand, subsequently causing the base of the table to come off the floor resulting in the reported event.The technician tested the function and operation of the 7080 surgical table and confirmed it to be operating to specifications.The technician also confirmed that no damage was noted to the table.The operator manual states, "warning - personal injury and/or equipment damage hazard- failure to keep all personnel and equipment clear of the surgical table before actuating any inertia-driven or power-driven movement could result in table damage and/or personal injury." a steris account manager offered in-service training on the proper use and operation of the 7080 surgical table specifically, the importance of ensuring equipment is clear of the table during articulations and is awaiting a response.The 7080 surgical table was returned to service.

• 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: 25694915
• Report Number: 1043572-2026-00061
• Device Sequence Number: 13198420
• Product Code: FQO
• UDI-Device Identifier: 00724995229139
• UDI-Public: (01)00724995229139(11)251211
• Combination Product (Y/N): N
• Initial Reporter State: FL
• 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): 07/02/2026

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: 06/04/2026
• Initial Report FDA Received Date: 07/02/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 12/11/2025
• 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