Product Wiki · Recalls · Health Canada

Eclipse — recall 21672

Health Canada · Canada · 2005-11-28 · Type III

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
Recall identifier
21672
Date of alert
2005-11-28
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
HC
Notice status
Archived by the issuing authority — kept for reference
Reported risk: A software anomaly which could result in an overdose to non-critical organs.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/eclipse

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.

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.