FDA recall record

OLEA MEDICAL Functional MR V1.0 recall — FDA Z-0122-2024

When exporting regions of interest in DICOM SEGMENTATION format, when simultaneously exporting multiple volumes of interest, a functional magnetic…

Class IIclassification
Z-0122-2024official record ID
Oct 25, 2023report date

Recall record at a glance

Official recordZ-0122-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOLEA MEDICAL
Report dateOct 25, 2023
Recall initiation dateAug 10, 2023
Quantity2
LocationLA CIOTAT, N/A, France

Official product description

Functional MR V1.0

Why the product was recalled

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 information

US: MI, MA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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