MAUDE Adverse Event Report: ELEKTA SOLUTIONS AB MOSAIQ; ACCELERATOR, LINEAR, MEDICAL

Medical Device Problem Code	Computer Software Problem (1112)
Health Effect - Clinical Code	Insufficient Information (4580)
Date of Event	08/11/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The manufacturer's investigation is on-going and further information will be provided once the investigation has completed.
Event or Problem Description
The customer reported a discrepancy between the treatment fields' parameters in mosaiq and the imported plans.
Additional Manufacturer Narrative
H2 updated.H6 updated.H10 updated.The investigation was completed by conducting a thorough evaluation of the product and the reported information.The customer reported a discrepancy between the treatment fields' parameters in mosaiq and the imported plans.Elekta used the same plan in-house provided by the customer to evaluate import processing and found that plan promotion works as expected.The parameter values (e.G., gantry, collimator, field size, etc.) in mosaiq matched those of the plan.Once promoted, the plan is in a pending state and values can be changed without version roll until the plan has been approved or treated.From the logs it was determined that changes by the user from the original plan occurred after the initial plan was imported and were accepted by the user.Based upon information available elekta physics have assessed that overall the patient received an underdose which is considered non-serious.The error led to an underdose of 50% to the intended region on two of four days of treatment.If this had been the only error the error in dose would be an underdose of 25%.This is expected to reduce the effectiveness of the treatment but is not expected to directly cause any significant health impact.The dose was not as intended on the other 2 days of treatment, however the dosimetric impact from the error in geometry on those days was smaller and does not further impact the assessment above.Mosaiq did not have any malfunction and worked as designed and intended.The issue was due to use error.

• Brand Name: MOSAIQ
• Common Device Name: ACCELERATOR, LINEAR, MEDICAL
• Manufacturer (Section D): ELEKTA SOLUTIONS AB; kungstensgatan 18; box 7593; stockholm, SE-10 3 93; SW SE-103 93
• Manufacturer (Section G): ELEKTA SOLUTIONS AB; 400 perimeter center terrace; suite 50; atlanta GA 30346
• Manufacturer Contact: cornerstone; london road; crawley, west sussex RH10 -9BL
• MDR Report Key: 17787362
• Report Number: 3015232217-2023-00059
• Device Sequence Number: 15314301
• Product Code: IYE
• UDI-Device Identifier: 00858164002282
• UDI-Public: (01)00858164002282(10)2.81.070
• Combination Product (Y/N): N
• Initial Reporter Country: VM
• PMA/510(K) Number: K183034
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Other,Foreign,Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 11/30/2023

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?: No
• Operator of Device: Health Professional
• 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: 08/22/2023
• Supplement Date Received by Manufacturer: 08/22/2023
• Initial Report FDA Received Date: 09/21/2023
• Supplement Report FDA Received Date: 11/30/2023
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/03/2019
• 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