MAUDE Adverse Event Report: Medivators Inc Advantage Plus Endoscope Reprocessing System

Model Number	1-2-510.003
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/20/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that the door to their advantage plus endoscope reprocessing system opened mid cycle and sprayed water.No report of injury.
Event or Problem Description
The user facility reported that the door to their advantage plus endoscope reprocessing system opened mid cycle and sprayed water.No report of injury.
Additional Manufacturer Narrative
The investigation of the reported event is in process.A follow-up report will be submitted once additional information becomes available.
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event to inspect the unit.The reported event could not be duplicated.To resolve the issue, the technician replaced the scu control board and the damaged temperature probe.The technician tested the unit, confirmed it to be operating according to specification, and returned it to service.The device history record was reviewed and confirmed the device was manufactured to specifications; no abnormalities were noted.A 3-year complaint review confirmed this to be an isolated event.No additional issues have been reported.

• Brand Name: Advantage Plus Endoscope Reprocessing System
• Common Device Name: Advantage Plus Endoscope Reprocessing System
• Manufacturer (Section D): Medivators Inc; 14605 28th avenue north; minneapolis MN 55447
• Manufacturer (Section G): Medivators Inc; 14605 28th avenue north; minneapolis MN 55447
• Manufacturer Contact: daniel davy ; 5960 heisley road; mentor, OH 44060 ; +1(440)259-7401
• MDR Report Key: 50300718
• Report Number: 2150060-2026-00037
• Device Sequence Number: 10698406
• Product Code: FEB
• UDI-Device Identifier: 00677964044755
• Combination Product (Y/N): N
• Initial Reporter Country: AS
• 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): 08/17/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 1-2-510.003
• Device Catalogue Number: 1-2-510.003
• 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: 07/20/2026
• Initial Report FDA Received Date: 08/18/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/14/2016
• 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