FDA Recall Open, Classified

GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.

Recall: Z-0750-2024 · Initiated November 30, 2023

Recall

Recall Number
Z-0750-2024
Event Number
93684
Firm
Xcision Medical Systems, LLC
FEI Number
3014273653
Product Code
IWB
Status
Open, Classified
Root Cause
Software design
Initiated
November 30, 2023
Posted
January 18, 2024
Address
9176 Red Branch Rd, Ste O, Columbia, MD, 21045-2001

Description

GammaPod - Treatment Planning System-a component of the GammaPod Irradiation System. Ref: XMSGP030A09.07-0.01 Intended for use in the noninvasive stereotactic delivery of a radiation dose to a partial volume of the breast in conjunction with breast conserving treatment.

Reason

Wrong structures imported into the GammaPod Treatment Planning System.-system allowed an RTSS generated from a previous CT scan to be selected

Action

Xcision issued Urgent Field Correction Letter via email on 11/30/23. Letter states reason for recall, health risk and action to take: Please post this notification internally for awareness of GammaPod BY CUSTOMER/USER Treatment Planning System users. Xcision is working on an update to the TPS software to implement controls to identify not only the patient identification but also the series of which the structures were delineated. This change is expected for implementation in early 2024. If you need any further information or support concerning this issue, please contact Xcision Customer Support at 855-924-7466 (1-855- SUPPORT XCISION).

Distribution

Worldwide - US Nationwide distribution in the states of MD, PA, TX and the country of Italy.

Quantity

4 units