MAUDE Adverse Event Report: ELEKTA INC MONACO; SYSTEM,PLANNING,RADIATION THERAPY TREATMENT

Medical Device Problem Code	Computer Software Problem (1112)
Health Effect - Clinical Code	No Patient Involvement (2645)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The investigation was completed by conducting a thorough evaluation of the product and the reported information.The issue was determined to be a defect in the product and will be fixed in a later version.
Event or Problem Description
The customer reported that monaco will display the incorrect mu for a 3d plan.Based on the available information there has been no mistreatment.

• Brand Name: MONACO
• Common Device Name: SYSTEM,PLANNING,RADIATION THERAPY TREATMENT
• Manufacturer (Section D): ELEKTA INC; 13723 riverport drive; suite 100; maryland heights MO 63043
• MDR Report Key: 7052006
• Report Number: 1937649-2017-00007
• Device Sequence Number: 94226
• Product Code: MUJ
• UDI-Device Identifier: 00858164002152
• UDI-Public: 00858164002152
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K151233
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,o
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 11/22/2017

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
• Was Device Available for Evaluation?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/26/2017
• Initial Report FDA Received Date: 11/22/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1