FDA Recall Open, Classified

Functional MR V1.0

Recall: Z-0122-2024 · Initiated August 10, 2023

Recall

Recall Number
Z-0122-2024
Event Number
93049
Firm
OLEA MEDICAL 93 AVANUE DU SORBIER, ZONE ATHELIA IV LA CIOTAT France
FEI Number
3007675959
Product Code
LLZ
Status
Open, Classified
Root Cause
Software design
Initiated
August 10, 2023
Posted
October 18, 2023

Description

Functional MR V1.0

Reason

When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic resonance software bug may cause file contents and associated series descriptions to not match, which could lead to a misinterpretation of clinical data.

Action

On 8/10/23, field safety notices were emailed to customers who were told to take the following actions: Advice for the user to detect if the bug occurred: This defect can be detected within the Functional MR V1.0 user interface by displaying the exported volume on an anatomical sequence. To detect the issue, the VOI shall be dragged and dropped from the data browser on an anatomical sequence, which will display a notification, indicating the original VOI s name. Outside of Functional MR V1.0 user interface, the user may check the DICOM tag "Segment Label (0062,0003)" in the viewer used, as this DICOM tag contains the correct VOI s name. Workaround: This problem can be overcome when exporting VOIs individually and has no impact on exporting VOIs merged with an anatomical map. New software will be available in October 2023. Complete and return the reply form via email to [email protected]

Distribution

US: MI, MA

Quantity

2