NeuViz 64 Multi-slice CT Scanner System Product Usage recall: Software Issue
NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system…
Why was NeuViz 64 Multi-slice CT Scanner System Product Usage recalled?
Software defect: For Helical scan with ClearView function, when small arc (uninterrupted scan) occurs during scan, there will be some electromagnetic interference in the system which may affect the control signal of the flying focal spot, resulting in an incorrect flying focal spot sequence. If the system does not receive error, it would continue to complete the scan with the incorrect flying focal spot sequence, having an effect on the reconstruction of some images, resulting in image loss.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
N64E120022E; N64E130039E; N641130051 E; N64E130062E; N64E130063E; N64E130066E;1 N641140077E; N64E140116E; N641140117E; N641140118E; N641140119E; N641140120E; N64EN150043E; N64E150121E; N64E150125E; N641150129E; N641150131 E; N641150136E; N641N160066E; N641N160067E; N64EN160068E; N64EN160071 E; N64EN160082E; N64EN160085E; N64EN160086E; N641N1 70093E; N641N1701 05E; N641N1 701 16E; N641N170120E; N641N170127E; N641N170128E; N641N170129E; N641N180156E; N641N180157E; N641N180161E; N641N180162E; N641N180205E
- Product
- NeuViz 64 Multi-slice CT Scanner System Product Usage: The Multi-Slice CT Scanner System can be used as a whole body computed tomography x-ray system…
- Recalling firm
- Neusoft Medical Systems Co., Ltd.
- Quantity
- 37
- Distribution
- US Nationwide Distribution.
- Recall date
- May 29, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)