Product Wiki · Recalls · Health Canada — Medical Devices

XVI and XVI R 4.5 (X-Ray Volume Imaging Systems), and XVI R 4.5 System — recall 51377

Health Canada — Medical Devices · Canada · 2014-03-25 · Type II

As described by Health Canada — Medical Devices: XVI and XVI R 4.5 (X-Ray Volume Imaging Systems), and XVI R 4.5 System - Upgrade Kit (2013-11-01)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
51377
Date of alert
2014-03-25
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Erroneous ASU table move in height direction may cause a collision when an external beam limiting device (BLD) (for example - Apex) is used.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/xvi-and-xvi-r-45-x-ray-volume-

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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