Product Wiki · Recalls · Health Canada — Medical Devices

Vicks Sinus Steam Inhaler (Vih200cv1) — recall 81644

Health Canada — Medical Devices · Canada · 2026-03-10 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
81644
Date of alert
2026-03-10
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Ear, nose and throat
Product type
Medical devices
Reported risk: The Vicks Sinus Steam Inhaler was distributed in Canada without the required Medical Device License (MDL) under the Health Canada medical devices regulations.
What you should do

Consumers are requested to hold on to the product and to call or email the consumer relations team at Kaz USA Inc., a Helen of Troy Company for questions related to their device. Consumer relations number (toll free): 1-800-827-6712 Weblink: https://www.helenoftroy.com/CONTACT-US/Email: [email protected]

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/vicks-sinus-steam-inhaler-vih2

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.