Alphenix INFX-8000v Main Unit
Brand(s)
Last updated
Summary
Product
Alphenix INFX-8000v Main Unit
Issue
Medical devices - Performance issue
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Alphenix INFX-8000v Main Unit |
Not applicable. |
INFX-8000V/PU |
Issue
It has been found that in combination with the x-ray flat panel detector (tfp-1200c), an unintended beam hardening filter would be selected in the x-ray beam limiting device.
Recall start date: le 12 juillet, 2022
Additional information
Details
Original published date: 2022-07-20
Alert / recall type
Health product recall
Category
Health products - Medical devices - Radiology
Companies
Canon Medical Systems Corporation
1385, Shimoishigami, Otawara-Shi, Tochigi-Ken, Japan, 324-8550
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-64378