Vicks Sinus Steam Inhaler Recalled in Canada Over Licensing Requirements
Kaz Usa, Inc. is recalling the Vicks Sinus Steam Inhaler (model VIH200CV1) because it was distributed in Canada without the required Medical Device License.
What Happened
Kaz Usa, Inc., a Helen of Troy Company, has issued a recall for the Vicks Sinus Steam Inhaler. According to Health Canada, the product was distributed throughout the Canadian market without the mandatory Medical Device License (MDL) required under the national medical devices regulations.
Which Products Are Affected
The recall involves the following product:
- Product Name: Vicks Sinus Steam Inhaler (Vih200cv1)
- Model Number: VIH200CV1
- Lot Numbers: All lots are affected
What You Should Do
Consumers who own the affected Vicks Sinus Steam Inhaler should identify if their device matches the model number VIH200CV1. While the recall notice focuses on the lack of regulatory licensing, consumers are advised to stay informed through official Health Canada updates regarding any further instructions for returns or disposal.
Why This Matters
Medical Device Licenses are a critical part of Health Canada’s regulatory framework, ensuring that health products sold to the public meet specific safety, quality, and effectiveness standards. Selling a device without this license means it has not undergone the necessary regulatory review for the Canadian market.
Source
For more information, visit the official Health Canada Recall Alert.
Source: Health Canada Official Notice