Product Wiki · Recalls · Health Canada — Marketed Health Products

Archived — recall 24162

Health Canada — Marketed Health Products · Canada · 2006-02-09

As described by Health Canada — Marketed Health Products: Archived - Implantable Pacemakers - Advisories, Warnings and Recalls for Health Professionals

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 — Marketed Health Products
Recall identifier
24162
Date of alert
2006-02-09
Country / jurisdiction
Canada
Risk type
recall
Product category
Medical devices
Product type
Marketed health products
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Two subsets of PULSAR ® MAX, PULSAR, DISCOVERY ® , MERIDIAN ® , PULSAR MAX II, DISCOVERY II, VIRTUS ® Plus II, INTELIS ® II and CONTAK ® TR implantable pacemakers
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/archived-implantable-pacemaker

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.

Related

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.