MAUDE Adverse Event Report: STERIS CORPORATION AMSCO; SURGICAL TABLE

Model Number	3085 SP SURGICAL TABLE
Medical Device Problem Code	Unintended Movement (3026)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/13/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that during the transfer of a patient, their 3085 surgical table "tipped slightly".The procedure was completed successfully.No report of injury.
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event to inspect the unit and found that one foot of the table was adjusted higher than the others which may have caused the reported event.The cause of the table foot being higher than the others could not be determined.To resolve the issue, the technician properly adjusted the foot of the table.The unit was tested, confirmed to be operating according to specification, and returned to service.The 3085 surgical table operator manual states, "verify power is on and table floor locks are properly engaged." the technician counseled user facility personnel on the proper use and operation of the 3085 surgical table.No additional issues have been reported.

• Brand Name: AMSCO
• 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: 24865947
• Report Number: 1043572-2026-00031
• Device Sequence Number: 16075593
• Product Code: FQO
• UDI-Device Identifier: 00724995155049
• UDI-Public: (01)00724995155049(11)181111
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: K971307
• 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): 04/13/2026

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: 3085 SP SURGICAL TABLE
• Device Catalogue Number: ST010101
• 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: 03/16/2026
• Initial Report FDA Received Date: 04/13/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/11/2018
• 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