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

Device Problem Computer Software Problem (1112)

Patient Problem Insufficient Information (4580)

Event Date 08/11/2023

Event Type  malfunction  

Event Description

The customer reported a discrepancy between the treatment fields' parameters in mosaiq and the imported plans.

Manufacturer Narrative

The manufacturer's investigation is on-going and further information will be provided once the investigation has completed.

Manufacturer Narrative

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 the overdose and considered this to be serious mistreatment from the perspective of percentage error in delivered dose.Based upon the information provided the error represents ~10% of the planned total mosaiq did not have any malfunction and worked as designed and intended.The issue was due to use error.

• Brand Name: MOSAIQ
• Type of Device: 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: 17787323
• MDR Text Key: 323895761
• Report Number: 3015232217-2023-00057
• Device Sequence Number: 1
• Product Code: IYE
• Combination Product (y/n): N
• Reporter Country Code: VM
• PMA/PMN Number: K183034
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other,Foreign,Health Professional,User Facility
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date: 12/01/2023

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
• Device Operator: Health Professional
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Initial Date Manufacturer Received: 08/22/2023
• Initial Date FDA Received: 09/21/2023
• Supplement Dates Manufacturer Received: 08/22/2023
• Supplement Dates FDA Received: 12/01/2023
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 10/03/2019
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1