MAUDE Adverse Event Report: Corporation Steris Canada Reliance; 6000 Series Reliance Endoscope Drying and Storage Cabinet

Model Number	6000 Series
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Laceration(s) (1946)
Date of Event	07/02/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
The user facility reported that employees sustained cuts to their arms while loading and unloading endoscopes from their 6000 series reliance endoscope drying and storage cabinet.It is unknown whether medical treatment was sought or administered.
Additional Manufacturer Narrative
The investigation into the reported event is in process.A follow-up report will be submitted when additional information becomes available.

• Brand Name: Reliance
• Common Device Name: 6000 Series Reliance Endoscope Drying and Storage Cabinet
• Manufacturer (Section D): Corporation Steris Canada; 490 boulevard armand-paris; quebec, G1C 8 A3; CA G1C 8A3
• Manufacturer (Section G): Corporation Steris Canada; 490 boulevard armand-paris; quebec, G1C 8 A3; CA G1C 8A3
• Manufacturer Contact: daniel davy ; 5960 heisley road; mentor, OH 44060 ; +1(440)259-7401
• MDR Report Key: 50097562
• Report Number: 9680353-2026-00033
• Device Sequence Number: 10317268
• Product Code: PUP
• UDI-Device Identifier: 00724995168124
• UDI-Public: (01)00724995168124
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• 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: 6000 Series
• Device Catalogue Number: REC6202DS
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 07/02/2026
• Initial Report FDA Received Date: 07/31/2026
• 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