Product Wiki · Recalls · Health Canada — Medical Devices

Intelepacs - Main Unit (2014-06-13) — recall 51986

Health Canada — Medical Devices · Canada · 2014-07-03 · Type II

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
51986
Date of alert
2014-07-03
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: In specific situations a partially truncated file may be written to the Intelepacs server. This partially truncated file can still be viewed by inteleviewer and inteleviewer will report to the user that the file in question is complete, when in fact they were looking at a glossy image.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/intelepacs-main-unit-2014-06-1

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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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.