Functional MR V1.0
FDA Recall Z-0122-2024 · Posted 2023-10-18
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Recalling FirmOLEA MEDICAL
Recall StatusOpen, Classified
Product CodeLLZ
Date Initiated2023-08-10
Product Quantity2
Reason for Recall
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.
Firm 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]
Root Cause
Software design
Distribution Pattern
US: MI, MA
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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