FDA recall record

Toshiba American Medical Systems EXCELART Vantage, Atlas, and Titan MRI Systems, MRT-1503 recall — FDA Z-2278-2012

The status display in the sequence queue window may not change from "Current" to "Done".

Class IIclassification
Z-2278-2012official record ID
Sep 5, 2012report date

Recall record at a glance

Official recordZ-2278-2012
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmToshiba American Medical Systems Inc.
Report dateSep 5, 2012
Recall initiation dateMay 13, 2008
Quantity54
LocationTustin, CA, United States

Official product description

EXCELART Vantage, Atlas, and Titan MRI Systems, MRT-1503 and MRT-1504. Imaging of the Whole Body, Fluid Visualization, 2D/3D Imaging, MR Angiography/MR Vascular Imaging, Blood Oxygenation Level Dependent Imaging, Perfusion I Diffusion Imaging, and Proton Spectroscopy.

Why the product was recalled

The status display in the sequence queue window may not change from "Current" to "Done".

Distribution information

Nationwide Distribution

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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