Health product recall

Alphenix INFX-8000v Main Unit

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 product - Medical device - 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