MAUDE Adverse Event Report: KARL STORZ SE & CO. KG UNIDRIVE S III MOTOR SYSTEM

Model Number	20701020-1
Medical Device Problem Code	Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	11/22/2024
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The affected device has been requested for investigation by the manufacturer.Device was not yet returned for investigation.The event is filed under internal karl storz complaint id: (b)(4).
Event or Problem Description
It was reported that the "foot pedal and morcellator unable to work with undriven, tested with 3 different morcellators but still has e09 error code.The customer rang whilst they were in a procedure and after advising to use another morcellator to see if the issue persists, she called back confirming the issue is still there and they had to cancel the case.

• Brand Name: UNIDRIVE S III MOTOR SYSTEM
• Common Device Name: UNIDRIVE S III MOTOR SYSTEM
• Manufacturer (Section D): KARL STORZ SE & CO. KG; dr.-karl-storz-strasse 34; tuttlingen, 78532 ; GM 78532
• MDR Report Key: 20869434
• Report Number: 2020550-2024-00496
• Device Sequence Number: 21026794
• Product Code: HIH
• UDI-Device Identifier: 04048551278802
• UDI-Public: 04048551278802
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Importer
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 12/06/2024
• Report Date (Section F): 12/06/2024

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?: Yes
• Operator of Device: Health Professional
• Device Model Number: 20701020-1
• Device Catalogue Number: 20701020-1
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Distributor Facility Aware Date: 12/05/2024
• Event Location: Hospital
• Date Report to Manufacturer: 12/06/2024
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 12/06/2024
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: MATERIAL: 20016230, SN: (B)(6).; MATERIAL: 27702050, SN: (B)(6)
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown