MAUDE Adverse Event Report: CORPORATION STERIS CANADA AMSCO; DRYING CABINET

Model Number	DRYING CABINET
Medical Device Problem Code	Connection Problem (2900)
Health Effect - Clinical Code	Electric Shock (2554)
Date of Event	04/21/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that an employee received a "light electric shock" while cleaning their amsco drying cabinet.No medical treatment was sought or administered and the employee continued working.
Additional Manufacturer Narrative
A steris service technician arrived onsite following the reported event and found that the amsco drying cabinet's power cord required replacement.The technician did not observe visible damage externally on the power cord or plug however, based on results of continuity testing the power cord may have exhibited internal damage.The technician removed the drying cabinet from service and is awaiting a replacement power cord.A 3-year complaint review confirmed this to be an isolated event.A follow-up report will be submitted when the drying cabinet is returned to service.

• Brand Name: AMSCO
• Common Device Name: DRYING 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 ; 4402597401
• MDR Report Key: 25243225
• Report Number: 9680353-2026-00025
• Device Sequence Number: 10500856
• Product Code: PUP
• UDI-Device Identifier: 00724995162610
• UDI-Public: (01)00724995162610
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 05/21/2026

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: DRYING CABINET
• Device Catalogue Number: DCR100101
• 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: 04/21/2026
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 05/21/2026
• Supplement Report FDA Received Date: 06/25/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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