Product Wiki · Recalls · Health Canada — Medical Devices

Alphenix INFX-8000v Main Unit — recall 64378

Health Canada — Medical Devices · Canada · 2022-07-18 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
64378
Date of alert
2022-07-18
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/alphenix-infx-8000v-main-unit

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