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FDA (Device enforcement)Recalled 2023-08-10class ii

OLEA MEDICAL: Functional MR V1.0

Hazard

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.

Details from the source

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. Distribution: US: MI, MA Quantity: 2 Lot/code info: UDI-DI: EOLEFMRIV1P00, Software Versions: V1.0, V1.0 SP1, V1.0 SP2, V1.0 SP3

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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