FDA recall record

NEUSOFT MEDICAL SYSTEMS IMP & EX NeuViz 128 Multi-slice CT Scanner System with software recall — FDA Z-0773-2019

For surview scan length more than 500mm,if the user aborts or skips the reconstructed surview, the image may have the wrong field of view (FOV). When user…

Class IIclassification
Z-0773-2019official record ID
Feb 13, 2019report date

Recall record at a glance

Official recordZ-0773-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNEUSOFT MEDICAL SYSTEMS IMP & EX
Report dateFeb 13, 2019
Recall initiation dateJan 9, 2019
Quantity3
LocationShenyang, China

Official product description

NeuViz 128 Multi-slice CT Scanner System with software version 1.0.8.5010O+P04 Vi .0.8.521 9+PO1 Multi-Slice CT Scanner System can be used as a whole body computed tomography X-ray system featuring a continuously rotating X-ray tube and detector array. The acquired X-RAY transmission data is reconstructed by computer into cross-sectional images of the body from either the same axial plane taken at different angles or spiral planes taken at different angles.

Why the product was recalled

For surview scan length more than 500mm,if the user aborts or skips the reconstructed surview, the image may have the wrong field of view (FOV). When user plans and performs subsequent clinical scan with the wrong FOV the actual start and end position may not be consistent with the planned positons.

Distribution information

US Distribution in states of: KS, OK and 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: FDA Mandated. 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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