Product Wiki · Recalls · Health Canada — Marketed Health Products

ZOFRAN (ondansetron) — recall 25707

Health Canada — Marketed Health Products · Canada · 2012-10-09

As described by Health Canada — Marketed Health Products: ZOFRAN (ondansetron) - Association with Changes in Electrical Activity in the Heart - 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
25707
Date of alert
2012-10-09
Country / jurisdiction
Canada
Risk type
recall
Product category
Drugs
Product type
Marketed health products
Notice status
Archived by the issuing authority — kept for reference
Reported risk: ZOFRAN ® (ondansetron hydrochloride dihydrate, ondansetron) - Important new safety information: Dose restriction for intravenous (IV) use due to dose-dependent QT interval prolongation
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/zofran-ondansetron-association

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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.