Product Wiki · Recalls · Health Canada Consumer Product Safety

Recall 22870 — Archived - Urgent Medical Device Information on Medtronic Sprint Fidelis Lead Recall and Patient Management Recommendations - Medtronic of Canada Ltd. - For the Public

Health Canada Consumer Product Safety · Canada · 2007-11-05

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Agency: Health Canada Consumer Product Safety
Recall identifier: 22870
Date of alert: 2007-11-05
Country / jurisdiction: Canada
Risk type: recall
Product category: Medical devices
Product type: Marketed health products

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/archived-urgent-medical-device

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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.

Recall 22870 — Archived - Urgent Medical Device Information on Medtronic Sprint Fidelis Lead Recall and Patient Management Recommendations - Medtronic of Canada Ltd. - For the Public

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