Changeflow GovPing Drug Safety Vicks Sinus Steam Inhaler Recall
Urgent Enforcement Removed Final

Vicks Sinus Steam Inhaler Recall

Favicon for recalls-rappels.canada.ca Health Canada Recalls & Safety Alerts
Filed February 25th, 2026
Detected March 10th, 2026
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Summary

Health Canada has issued a recall for the Vicks Sinus Steam Inhaler (VIH200CV1) because it was distributed without the required Medical Device License. Consumers are advised to retain the product and contact Kaz USA Inc. for further instructions.

What changed

Health Canada has announced a recall for the Vicks Sinus Steam Inhaler (Model VIH200CV1) due to it being an unauthorized medical device. The product was distributed in Canada without the necessary Medical Device License, violating Health Canada's regulations. The affected lot number is 17824.

Consumers who have purchased this product are instructed to hold onto it and contact Kaz USA Inc., a Helen of Troy Company, via their consumer relations team by phone (1-800-827-6712) or email (bwconsumersupport@cs.helenoftroy.com) for questions regarding their device. This recall is classified as Type II, indicating a potential risk to health.

What to do next

  1. Consumers should retain the product and contact Kaz USA Inc. for further instructions.
  2. Review product distribution records to ensure compliance with Medical Device Licensing requirements.

Source document (simplified)

Health product recall

Vicks Sinus Steam Inhaler (Vih200cv1)

Brand(s)

Kaz Usa, Inc., A Helen Of Troy Company

Last updated

2026-03-09

Summary

Product Vicks Sinus Steam Inhaler (Vih200cv1) Issue Medical devices - Unauthorised device What to 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.

Affected products

| Affected products | Lot or serial number | Model or catalogue number |
| --- | --- | --- |
| Vicks Sinus Steam Inhaler (Vih200cv1) | 17824 | VIH200CV1 |

Issue

The Vicks Sinus Steam Inhaler was distributed in Canada without the required Medical Device License (MDL) under the Health Canada medical devices regulations.

Additional information

Details

Original published date:

2026-02-25

Alert / recall type Health product recall Category Health products - Medical devices - Ear, nose and throat Companies Kaz Usa, Inc., A Helen Of Troy Company

400 Donald Lynch Boulevard, Marlborough, Massachusetts, United States, 01752

Published by Health Canada Audience General public Industry Recall class Type II Recall date

2026-02-03

Identification number RA-81644

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Source

Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
Various Canadian Agencies
Filed
February 25th, 2026
Instrument
Enforcement
Legal weight
Binding
Stage
Final
Change scope
Substantive

Who this affects

Applies to
Consumers Manufacturers
Geographic scope
National (Canada)

Taxonomy

Primary area
Medical Devices
Operational domain
Compliance
Topics
Product Safety Recalls

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